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Pediatric Disease Annotations & Medicines



   gestational diabetes
  

Disease ID 665
Disease gestational diabetes
Definition
Diabetes mellitus induced by PREGNANCY but resolved at the end of pregnancy. It does not include previously diagnosed diabetics who become pregnant (PREGNANCY IN DIABETICS). Gestational diabetes usually develops in late pregnancy when insulin antagonistic hormones peaks leading to INSULIN RESISTANCE; GLUCOSE INTOLERANCE; and HYPERGLYCEMIA.
Synonym
#NAME?
diabetes and pregnancy
diabetes during pregnancy
diabetes gestatational
diabetes mellitus (gestational)
diabetes mellitus arising in pregnancy
diabetes mellitus, gestational
diabetes pregn ind
diabetes, gestational
diabetes, gestational [disease/finding]
diabetes, pregnancy induced
diabetes, pregnancy-induced
gdm
gdm - gestational diabetes mellitus
gestational diabetes mellitus
gestational diabetes mellitus (disorder)
gestational diabetes mellitus, nos
maternal diabetes
maternal gestational diabetes mellitus
maternal gestational diabetes mellitus (disorder)
pregnancy induced diabetes
pregnancy-induced diabetes
DOID
UMLS
C0085207
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:49)
C0011847  |  diabetes  |  44
C0028754  |  obesity  |  22
C0011860  |  type 2 diabetes  |  15
C0020538  |  hypertension  |  12
C0020538  |  hypertensive disorder  |  10
C0011849  |  diabetes mellitus  |  6
C0271650  |  glucose intolerance  |  6
C0032460  |  polycystic ovary syndrome  |  4
C0013537  |  eclampsia  |  4
C0032460  |  polycystic ovary  |  4
C0948265  |  metabolic syndrome  |  3
C0032460  |  polycystic ovarian syndrome  |  3
C0011854  |  type 1 diabetes  |  3
C0032914  |  preeclampsia  |  3
C0028754  |  adiposity  |  3
C0020456  |  hyperglycemia  |  3
C0015938  |  fetal macrosomia  |  2
C0042870  |  vitamin d defic  |  2
C0042870  |  vitamin d deficiency  |  2
C0085207  |  maternal diabetes  |  2
C0003467  |  anxiety  |  2
C0162739  |  hellp syndrome  |  2
C0011860  |  type 2 diabetes mellitus  |  2
C0011570  |  depression  |  2
C0011880  |  diabetic ketoacidosis  |  1
C0011860  |  maturity onset diabetes  |  1
C0011854  |  type 1 diabetes mellitus  |  1
C0032460  |  polycystic ovaries  |  1
C0021390  |  inflammatory bowel disease  |  1
C1704437  |  respiratory distress syndrome  |  1
C0007194  |  hypertrophic cardiomyopathy  |  1
C0032051  |  placental insufficiency  |  1
C0000786  |  miscarriage  |  1
C0013418  |  dystocia  |  1
C0878544  |  cardiomyopathy  |  1
C0004153  |  atherosclerosis  |  1
C0021831  |  bowel disease  |  1
C0037315  |  sleep apnea  |  1
C0271650  |  prediabetes  |  1
C0159069  |  impaired glucose tolerance  |  1
C0000832  |  placental abruption  |  1
C0020676  |  hypothyroid  |  1
C0564778  |  obstetrical complications  |  1
C0022658  |  renal disease  |  1
C0849777  |  cystic ovaries  |  1
C0340274  |  gestational hypertension  |  1
C0031099  |  periodontitis  |  1
C0154251  |  lipid disorders  |  1
C0020459  |  hyperinsulinism  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:12)
SOD2  |  6648  |  CTD_human
GCK  |  2645  |  CLINVAR
LEP  |  3952  |  CTD_human
ADIPOQ  |  9370  |  CTD_human
CYP19A1  |  1588  |  CTD_human
AR  |  367  |  CTD_human
LEPR  |  3953  |  CTD_human
SIRT3  |  23410  |  CTD_human
MBL2  |  4153  |  CTD_human
FGF2  |  2247  |  CTD_human
IGF2BP2  |  10644  |  GWASCAT
CDKAL1  |  54901  |  GWASCAT
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:26)
6833  |  ABCC8  |  infer
9370  |  ADIPOQ  |  infer
155  |  ADRB3  |  infer
11132  |  CAPN10  |  infer
54901  |  CDKAL1  |  infer
2303  |  FOXC2  |  infer
2645  |  GCK  |  infer
3117  |  HLA-DQA1  |  infer
3119  |  HLA-DQB1  |  infer
3123  |  HLA-DRB1  |  infer
3127  |  HLA-DRB5  |  infer
3133  |  HLA-E  |  infer
3172  |  HNF4A  |  infer
10644  |  IGF2BP2  |  infer
3630  |  INS  |  infer
3667  |  IRS1  |  infer
3767  |  KCNJ11  |  infer
5468  |  PPARG  |  infer
10891  |  PPARGC1A  |  infer
100271597  |  RPS3AP42  |  infer
5054  |  SERPINE1  |  infer
6934  |  TCF7L2  |  infer
10911  |  UTS2  |  infer
4153  |  MBL2  |  infer
3481  |  IGF2  |  infer
3643  |  INSR  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:291)
104940698  |  DALIR  |  DISEASES
6894  |  TARBP1  |  DISEASES
9603  |  NFE2L3  |  DISEASES
6515  |  SLC2A3  |  DISEASES
3784  |  KCNQ1  |  DISEASES
10272  |  FSTL3  |  DISEASES
4335  |  MNT  |  DISEASES
1361  |  CPB2  |  DISEASES
5603  |  MAPK13  |  DISEASES
4282  |  MIF  |  DISEASES
3956  |  LGALS1  |  DISEASES
1591  |  CYP24A1  |  DISEASES
5020  |  OXT  |  DISEASES
57136  |  APMAP  |  DISEASES
366  |  AQP9  |  DISEASES
5327  |  PLAT  |  DISEASES
8797  |  TNFRSF10A  |  DISEASES
56729  |  RETN  |  DISEASES
26291  |  FGF21  |  DISEASES
5444  |  PON1  |  DISEASES
10135  |  NAMPT  |  DISEASES
3199  |  HOXA2  |  DISEASES
3955  |  LFNG  |  DISEASES
5054  |  SERPINE1  |  DISEASES
5919  |  RARRES2  |  DISEASES
2645  |  GCK  |  DISEASES
8721  |  EDF1  |  DISEASES
11101  |  ATE1  |  DISEASES
6347  |  CCL2  |  DISEASES
5539  |  PPY  |  DISEASES
1594  |  CYP27B1  |  DISEASES
338  |  APOB  |  DISEASES
5624  |  PROC  |  DISEASES
335  |  APOA1  |  DISEASES
9429  |  ABCG2  |  DISEASES
3375  |  IAPP  |  DISEASES
50835  |  TAS2R9  |  DISEASES
847  |  CAT  |  DISEASES
6745  |  SSR1  |  DISEASES
2806  |  GOT2  |  DISEASES
51141  |  INSIG2  |  DISEASES
57152  |  SLURP1  |  DISEASES
57794  |  SUGP1  |  DISEASES
7103  |  TSPAN8  |  DISEASES
2678  |  GGT1  |  DISEASES
7166  |  TPH1  |  DISEASES
3630  |  INS  |  DISEASES
3040  |  HBA2  |  DISEASES
2056  |  EPO  |  DISEASES
9945  |  GFPT2  |  DISEASES
1401  |  CRP  |  DISEASES
1116  |  CHI3L1  |  DISEASES
2167  |  FABP4  |  DISEASES
54407  |  SLC38A2  |  DISEASES
4544  |  MTNR1B  |  DISEASES
10993  |  SDS  |  DISEASES
6927  |  HNF1A  |  DISEASES
79074  |  C2orf49  |  DISEASES
3569  |  IL6  |  DISEASES
2572  |  GAD2  |  DISEASES
2998  |  GYS2  |  DISEASES
9388  |  LIPG  |  DISEASES
6532  |  SLC6A4  |  DISEASES
23071  |  ERP44  |  DISEASES
28965  |  SLC27A6  |  DISEASES
8178  |  ELL  |  DISEASES
25939  |  SAMHD1  |  DISEASES
1109  |  AKR1C4  |  DISEASES
3553  |  IL1B  |  DISEASES
23476  |  BRD4  |  DISEASES
4722  |  NDUFS3  |  DISEASES
3791  |  KDR  |  DISEASES
3383  |  ICAM1  |  DISEASES
10891  |  PPARGC1A  |  DISEASES
26998  |  FETUB  |  DISEASES
4717  |  NDUFC1  |  DISEASES
51083  |  GAL  |  DISEASES
11062  |  DUS4L  |  DISEASES
409  |  ARRB2  |  DISEASES
57332  |  CBX8  |  DISEASES
207  |  AKT1  |  DISEASES
8547  |  FCN3  |  DISEASES
8915  |  BCL10  |  DISEASES
52  |  ACP1  |  DISEASES
29114  |  TAGLN3  |  DISEASES
5295  |  PIK3R1  |  DISEASES
54901  |  CDKAL1  |  DISEASES
79017  |  GGCT  |  DISEASES
3484  |  IGFBP1  |  DISEASES
2041  |  EPHA1  |  DISEASES
5047  |  PAEP  |  DISEASES
23389  |  MED13L  |  DISEASES
2321  |  FLT1  |  DISEASES
1834  |  DSPP  |  DISEASES
3087  |  HHEX  |  DISEASES
5468  |  PPARG  |  DISEASES
5675  |  PSG6  |  DISEASES
563  |  AZGP1  |  DISEASES
115290  |  FBXO17  |  DISEASES
178  |  AGL  |  DISEASES
7412  |  VCAM1  |  DISEASES
23498  |  HAAO  |  DISEASES
5798  |  PTPRN  |  DISEASES
213  |  ALB  |  DISEASES
327  |  APEH  |  DISEASES
222962  |  SLC29A4  |  DISEASES
4846  |  NOS3  |  DISEASES
2636  |  GBX1  |  DISEASES
57094  |  CPA6  |  DISEASES
360  |  AQP3  |  DISEASES
10999  |  SLC27A4  |  DISEASES
55181  |  SMG8  |  DISEASES
4054  |  LTBP3  |  DISEASES
51282  |  SCAND1  |  DISEASES
5617  |  PRL  |  DISEASES
203190  |  LGI3  |  DISEASES
3479  |  IGF1  |  DISEASES
4543  |  MTNR1A  |  DISEASES
375444  |  C5orf34  |  DISEASES
3643  |  INSR  |  DISEASES
121355  |  GTSF1  |  DISEASES
3667  |  IRS1  |  DISEASES
8862  |  APLN  |  DISEASES
84684  |  INSM2  |  DISEASES
5340  |  PLG  |  DISEASES
7534  |  YWHAZ  |  DISEASES
51316  |  PLAC8  |  DISEASES
1444  |  CSHL1  |  DISEASES
763  |  CA5A  |  DISEASES
4023  |  LPL  |  DISEASES
27165  |  GLS2  |  DISEASES
162515  |  SLC16A11  |  DISEASES
56945  |  MRPS22  |  DISEASES
407  |  ARR3  |  DISEASES
3952  |  LEP  |  DISEASES
2688  |  GH1  |  DISEASES
3172  |  HNF4A  |  DISEASES
1442  |  CSH1  |  DISEASES
55095  |  SAMD4B  |  DISEASES
282679  |  AQP11  |  DISEASES
9370  |  ADIPOQ  |  DISEASES
6517  |  SLC2A4  |  DISEASES
3992  |  FADS1  |  DISEASES
3039  |  HBA1  |  DISEASES
6514  |  SLC2A2  |  DISEASES
55600  |  ITLN1  |  DISEASES
146802  |  SLC47A2  |  DISEASES
5831  |  PYCR1  |  DISEASES
326340  |  ZAR1  |  DISEASES
3953  |  LEPR  |  DISEASES
254887  |  ZDHHC23  |  DISEASES
5069  |  PAPPA  |  DISEASES
6401  |  SELE  |  DISEASES
25825  |  BACE2  |  DISEASES
2689  |  GH2  |  DISEASES
340075  |  ARSI  |  DISEASES
130574  |  LYPD6  |  DISEASES
120227  |  CYP2R1  |  DISEASES
51738  |  GHRL  |  DISEASES
10363  |  HMG20A  |  DISEASES
9376  |  SLC22A8  |  DISEASES
1551  |  CYP3A7  |  DISEASES
10239  |  AP3S2  |  DISEASES
7335  |  UBE2V1  |  DISEASES
392636  |  AGMO  |  DISEASES
51094  |  ADIPOR1  |  DISEASES
2804  |  GOLGB1  |  DISEASES
132660  |  LIN54  |  DISEASES
145264  |  SERPINA12  |  DISEASES
2305  |  FOXM1  |  DISEASES
9031  |  BAZ1B  |  DISEASES
28986  |  MAGEH1  |  DISEASES
155  |  ADRB3  |  DISEASES
8720  |  MBTPS1  |  DISEASES
3638  |  INSIG1  |  DISEASES
1465  |  CSRP1  |  DISEASES
3767  |  KCNJ11  |  DISEASES
3921  |  RPSA  |  DISEASES
10920  |  COPS8  |  DISEASES
80201  |  HKDC1  |  DISEASES
6720  |  SREBF1  |  DISEASES
79602  |  ADIPOR2  |  DISEASES
987  |  LRBA  |  DISEASES
7323  |  UBE2D3  |  DISEASES
2695  |  GIP  |  DISEASES
3177  |  SLC29A2  |  DISEASES
55621  |  TRMT1  |  DISEASES
871  |  SERPINH1  |  DISEASES
9464  |  HAND2  |  DISEASES
145864  |  HAPLN3  |  DISEASES
116969  |  ART5  |  DISEASES
2673  |  GFPT1  |  DISEASES
2475  |  MTOR  |  DISEASES
4283  |  CXCL9  |  DISEASES
79674  |  VEPH1  |  DISEASES
4514  |  MT-CO3  |  DISEASES
22796  |  COG2  |  DISEASES
81788  |  NUAK2  |  DISEASES
3814  |  KISS1  |  DISEASES
777  |  CACNA1E  |  DISEASES
632  |  BGLAP  |  DISEASES
117247  |  SLC16A10  |  DISEASES
54855  |  FAM46C  |  DISEASES
51167  |  CYB5R4  |  DISEASES
83699  |  SH3BGRL2  |  DISEASES
6319  |  SCD  |  DISEASES
11147  |  HHLA3  |  DISEASES
56889  |  TM9SF3  |  DISEASES
5950  |  RBP4  |  DISEASES
2030  |  SLC29A1  |  DISEASES
84879  |  MFSD2A  |  DISEASES
252995  |  FNDC5  |  DISEASES
65108  |  MARCKSL1  |  DISEASES
553115  |  PEF1  |  DISEASES
4153  |  MBL2  |  DISEASES
2268  |  FGR  |  DISEASES
3339  |  HSPG2  |  DISEASES
55920  |  RCC2  |  DISEASES
3055  |  HCK  |  DISEASES
8660  |  IRS2  |  DISEASES
10927  |  SPIN1  |  DISEASES
55937  |  APOM  |  DISEASES
9358  |  ITGBL1  |  DISEASES
1880  |  GPR183  |  DISEASES
8718  |  TNFRSF25  |  DISEASES
10159  |  ATP6AP2  |  DISEASES
3980  |  LIG3  |  DISEASES
51374  |  ATRAID  |  DISEASES
551  |  AVP  |  DISEASES
3045  |  HBD  |  DISEASES
6462  |  SHBG  |  DISEASES
3030  |  HADHA  |  DISEASES
6541  |  SLC7A1  |  DISEASES
2762  |  GMDS  |  DISEASES
55623  |  THUMPD1  |  DISEASES
5618  |  PRLR  |  DISEASES
55203  |  LGI2  |  DISEASES
10644  |  IGF2BP2  |  DISEASES
1133  |  CHRM5  |  DISEASES
348801  |  LNP1  |  DISEASES
9467  |  SH3BP5  |  DISEASES
4017  |  LOXL2  |  DISEASES
653247  |  PRB2  |  DISEASES
6710  |  SPTB  |  DISEASES
6833  |  ABCC8  |  DISEASES
3898  |  LAD1  |  DISEASES
11132  |  CAPN10  |  DISEASES
1443  |  CSH2  |  DISEASES
116985  |  ARAP1  |  DISEASES
174  |  AFP  |  DISEASES
55233  |  MOB1A  |  DISEASES
144195  |  SLC2A14  |  DISEASES
9373  |  PLAA  |  DISEASES
81539  |  SLC38A1  |  DISEASES
3119  |  HLA-DQB1  |  DISEASES
1607  |  DGKB  |  DISEASES
375704  |  ENHO  |  DISEASES
27124  |  INPP5J  |  DISEASES
5672  |  PSG4  |  DISEASES
7441  |  VPREB1  |  DISEASES
728441  |  GGT2  |  DISEASES
7018  |  TF  |  DISEASES
2641  |  GCG  |  DISEASES
3120  |  HLA-DQB2  |  DISEASES
3481  |  IGF2  |  DISEASES
197  |  AHSG  |  DISEASES
1029  |  CDKN2A  |  DISEASES
7124  |  TNF  |  DISEASES
10216  |  PRG4  |  DISEASES
5706  |  PSMC6  |  DISEASES
6829  |  SUPT5H  |  DISEASES
219537  |  SMTNL1  |  DISEASES
115098  |  CCDC124  |  DISEASES
100131827  |  ZNF717  |  DISEASES
408  |  ARRB1  |  DISEASES
7555  |  CNBP  |  DISEASES
3586  |  IL10  |  DISEASES
169026  |  SLC30A8  |  DISEASES
6513  |  SLC2A1  |  DISEASES
28988  |  DBNL  |  DISEASES
79068  |  FTO  |  DISEASES
25907  |  TMEM158  |  DISEASES
6934  |  TCF7L2  |  DISEASES
7421  |  VDR  |  DISEASES
8972  |  MGAM  |  DISEASES
283450  |  HECTD4  |  DISEASES
387521  |  TMEM189  |  DISEASES
56342  |  PPAN  |  DISEASES
5228  |  PGF  |  DISEASES
83608  |  C18orf21  |  DISEASES
283120  |  H19  |  DISEASES
Locus(Waiting for update.)
Disease ID 665
Disease gestational diabetes
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:49)
HP:0001513  |  Obesity  |  21
HP:0000855  |  Insulin resistance  |  16
HP:0000822  |  Hypertension  |  12
HP:0001520  |  Birthweight > 90th percentile  |  10
HP:0000833  |  Glucose intolerance  |  6
HP:0000819  |  Diabetes mellitus  |  6
HP:0000147  |  Sclerocystic ovaries  |  5
HP:0003074  |  High blood glucose  |  3
HP:0002960  |  Autoimmune condition  |  3
HP:0100601  |  Eclampsia  |  3
HP:0100602  |  Pre-eclampsia  |  3
HP:0001824  |  Weight loss  |  3
HP:0001622  |  Premature delivery  |  2
HP:0000739  |  Anxiety  |  2
HP:0000716  |  Depression  |  2
HP:0009800  |  gestational diabetes  |  2
HP:0001952  |  Abnormal glucose tolerance  |  2
HP:0001518  |  Small for gestational age  |  2
HP:0001788  |  Premature rupture of membranes  |  2
HP:0100512  |  Vitamin D deficiency  |  2
HP:0000078  |  Genital abnormalities  |  2
HP:0001993  |  Ketoacidosis  |  2
HP:0001548  |  Overgrowth  |  2
HP:0100603  |  Toxemia of pregnancy  |  2
HP:0009058  |  Muscle lipidosis  |  1
HP:0001953  |  Diabetic ketosis  |  1
HP:0011413  |  Shoulder dystocia  |  1
HP:0010535  |  Sleep apnea  |  1
HP:0001397  |  Hepatic steatosis  |  1
HP:0001507  |  Abnormal growth  |  1
HP:0002104  |  Absence of spontaneous respiration  |  1
HP:0001638  |  Cardiomyopathy  |  1
HP:0011419  |  Abruptio placentae  |  1
HP:0001988  |  hypoglycemia, recurrent  |  1
HP:0000159  |  Lip abnormality  |  1
HP:0001511  |  Prenatal onset growth retardation  |  1
HP:0006279  |  Beta-cell dysfunction  |  1
HP:0100543  |  Cognitive deficits  |  1
HP:0002098  |  Respiratory distress  |  1
HP:0004904  |  Maturity-onset diabetes of the young  |  1
HP:0030216  |  Inertia  |  1
HP:0001631  |  Atria septal defect  |  1
HP:0011675  |  Arrhythmias  |  1
HP:0002621  |  Atherosclerosis  |  1
HP:0000704  |  Pyorrhea  |  1
HP:0012594  |  High urine albumin levels  |  1
HP:0002529  |  Neuronal loss in central nervous system  |  1
HP:0001639  |  Hypertrophic cardiomyopathy  |  1
HP:0000138  |  Ovarian cyst  |  1
Disease ID 665
Disease gestational diabetes
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:4)
C0020538  |  hypertension  |  12
C0271650  |  glucose intolerance  |  5
C0032962  |  pregnancy complications  |  3
C0015938  |  fetal macrosomia  |  2
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:240)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs10010131189846647466WFS1umls:C0085207BeFreeAll the risk alleles in the 11 examined type 2 diabetes risk variants showed an odds ratio (OR) greater than 1 for the GDM group compared with the control group ranging from 1.13 [95% confidence interval (CI) 0.88-1.46] to 1.44 (95% CI 1.19-1.74) except for the WFS1 rs10010131 variant with OR 0.87 (95% CI 0.73-1.05).0.0002714422009WFS146291188AG
rs1007888257300194282MIFumls:C0085207BeFreeAssociation between macrophage migration inhibitory factor rs1007888 and GDM.0.0005428842016MIF-AS12223898914CT
rs10811661190024303087HHEXumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009NA922134095TC
rs10811661190024301030CDKN2Bumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009NA922134095TC
rs108116611900243054901CDKAL1umls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.1234527992009NA922134095TC
rs10811661190024301029CDKN2Aumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009NA922134095TC
rs10811661190024303630INSumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0238208712009NA922134095TC
rs10811661225917073767KCNJ11umls:C0085207BeFree13 SNPs (FTO rs8050136, CDKAL1 rs7754840 and rs7756992, CDKN2A/2B rs10811661, HHEX rs1111875, IGF2BP2 rs1470579 and rs4402960, SLC30A8 rs13266634, TCF7L2 rs7903146, PPARG rs1801282, GCK rs1799884, HNF1A rs1169288, and KCNJ11 rs5219) were genotyped in 793 women with GDM after a median follow-up of 57 months.0.0091729422012NA922134095TC
rs10830963247281283630INSumls:C0085207BeFreers10830963 was associated cross-sectionally with fasting glucose (p = 0.0069), acute insulin response (AIR; p = 0.0013), disposition index (p = 0.00078), glucose effectiveness (p = 0.018) and gestational diabetes mellitus (OR 1.48; p = 0.012), but not with OGTT 30 min Δinsulin (the difference between the 30 min and fasting plasma insulin concentration) or 30 min insulin-based disposition index.0.0238208712014MTNR1B1192975544CG
rs10830963236903053667IRS1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0053528932013MTNR1B1192975544CG
rs10830963220965103630INSumls:C0085207BeFreeWe also found that the risk alleles of rs2383208 (b = -0.085, p = 0.003), rs4402960 (b = -0.057, p = 0.046) and rs10830963 (b = -0.096, p = 0.001) were associated with HOMA-B, while rs7754840 was associated with decrease in insulin AUC during a 100 g OGTT given at the time of GDM diagnosis (b = -0.080, p = 0.007).0.0238208712011MTNR1B1192975544CG
rs108309632369030554901CDKAL1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1234527992013MTNR1B1192975544CG
rs10830963224503464544MTNR1Bumls:C0085207BeFreeThe rs10830963 variant of melatonin receptor MTNR1B is associated with increased risk for gestational diabetes mellitus in a Greek population.0.0021715352012MTNR1B1192975544CG
rs10830963234569076934TCF7L2umls:C0085207BeFreeAmong Caucasian women, GDM was associated with carriage of TCF7L2 rs7901695, MTNR1B rs10830963 and GCKR rs780094 alleles that are associated with T2DM and fasting glucose in nonpregnant populations.0.0142543932014MTNR1B1192975544CG
rs10830963236903054544MTNR1Bumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0021715352013MTNR1B1192975544CG
rs10830963236903053767KCNJ11umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0091729422013MTNR1B1192975544CG
rs108309632369030510644IGF2BP2umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.125548392013MTNR1B1192975544CG
rs10830963236903052645GCKumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1448082882013MTNR1B1192975544CG
rs1111875190024301029CDKN2Aumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009NA1092703125CT
rs1111875190024303087HHEXumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009NA1092703125CT
rs11118751900243054901CDKAL1umls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.1234527992009NA1092703125CT
rs1111875190024303630INSumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0238208712009NA1092703125CT
rs1111875225917073767KCNJ11umls:C0085207BeFree13 SNPs (FTO rs8050136, CDKAL1 rs7754840 and rs7756992, CDKN2A/2B rs10811661, HHEX rs1111875, IGF2BP2 rs1470579 and rs4402960, SLC30A8 rs13266634, TCF7L2 rs7903146, PPARG rs1801282, GCK rs1799884, HNF1A rs1169288, and KCNJ11 rs5219) were genotyped in 793 women with GDM after a median follow-up of 57 months.0.0091729422012NA1092703125CT
rs1111875190024301030CDKN2Bumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009NA1092703125CT
rs1169288225917073767KCNJ11umls:C0085207BeFree13 SNPs (FTO rs8050136, CDKAL1 rs7754840 and rs7756992, CDKN2A/2B rs10811661, HHEX rs1111875, IGF2BP2 rs1470579 and rs4402960, SLC30A8 rs13266634, TCF7L2 rs7903146, PPARG rs1801282, GCK rs1799884, HNF1A rs1169288, and KCNJ11 rs5219) were genotyped in 793 women with GDM after a median follow-up of 57 months.0.0091729422012HNF1A12120978847AC
rs1169288167521736927HNF1Aumls:C0085207BeFreeThe -30G-->A polymorphism of the beta-cell-specific promoter of GCK and the I27L polymorphism of HNF1A seem to increase the risk of GDM in Scandinavian women.0.0106397722006HNF1A12120978847AC
rs1169288167521732645GCKumls:C0085207BeFreeThe -30G-->A polymorphism of the beta-cell-specific promoter of GCK and the I27L polymorphism of HNF1A seem to increase the risk of GDM in Scandinavian women.0.1448082882006HNF1A12120978847AC
rs1169288167521735871MAP4K2umls:C0085207BeFreeThe -30G-->A polymorphism of the beta-cell-specific promoter of GCK and the I27L polymorphism of HNF1A seem to increase the risk of GDM in Scandinavian women.0.0005428842006HNF1A12120978847AC
rs11708067237614237088TLE1umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013ADCY53123346931AG
rs1170806723761423111ADCY5umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013ADCY53123346931AG
rs11708067237614236934TCF7L2umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0142543932013ADCY53123346931AG
rs11708067237614232646GCKRumls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013ADCY53123346931AG
rs117080672376142357818G6PC2umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013ADCY53123346931AG
rs117080672376142379068FTOumls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0005428842013ADCY53123346931AG
rs12243326259739436934TCF7L2umls:C0085207BeFreeAssociation with GDM was found for two of the most frequently replicated T2D loci: a TCF7L2 haplotype (CTTC: rs7901695, rs4506565, rs7903146, rs12243326; P=2.16 x 10(-06); OR=2.95) and a KCNQ1 haplotype (TTT: rs2237892, rs163184, rs2237897; P=1.98 x 10(-05); OR=0.55).0.0142543932015TCF7L210113029056TC
rs12255372236903052645GCKumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1448082882013TCF7L210113049143GT
rs122553722369030554901CDKAL1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1234527992013TCF7L210113049143GT
rs12255372236903053667IRS1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0053528932013TCF7L210113049143GT
rs122553722369030510644IGF2BP2umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.125548392013TCF7L210113049143GT
rs12255372236903053767KCNJ11umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0091729422013TCF7L210113049143GT
rs12255372236903056934TCF7L2umls:C0085207BeFreeAmong them, genetic variants in TCF7L2 showed the strongest association with GDM risk, with ORs (95% CIs) of 1.44 (1.29-1.60, P < 0.001) per T allele of rs7903146 and 1.46 (1.15-1.84, P = 0.002) per T allele of rs12255372.0.0142543932013TCF7L210113049143GT
rs12255372236903054544MTNR1Bumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0021715352013TCF7L210113049143GT
rs13266634225917073767KCNJ11umls:C0085207BeFree13 SNPs (FTO rs8050136, CDKAL1 rs7754840 and rs7756992, CDKN2A/2B rs10811661, HHEX rs1111875, IGF2BP2 rs1470579 and rs4402960, SLC30A8 rs13266634, TCF7L2 rs7903146, PPARG rs1801282, GCK rs1799884, HNF1A rs1169288, and KCNJ11 rs5219) were genotyped in 793 women with GDM after a median follow-up of 57 months.0.0091729422012SLC30A8;LOC1053757168117172544CT
rs137852671200420136833ABCC8umls:C0085207BeFreeHyperinsulinemic hypoglycemia evolving to gestational diabetes and diabetes mellitus in a family carrying the inactivating ABCC8 E1506K mutation.0.0031813582010ABCC81117394295CT
rs1387153236903053767KCNJ11umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0091729422013NA1192940662CT
rs1387153236903053667IRS1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0053528932013NA1192940662CT
rs1387153236903054544MTNR1Bumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0021715352013NA1192940662CT
rs13871532369030510644IGF2BP2umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.125548392013NA1192940662CT
rs1387153236903052645GCKumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1448082882013NA1192940662CT
rs13871532369030554901CDKAL1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1234527992013NA1192940662CT
rs14705792223365110644IGF2BP2umls:C0085207GWASCATA genome-wide association study of gestational diabetes mellitus in Korean women.0.125548392012IGF2BP23185811292AC
rs14705792223365110644IGF2BP2umls:C0085207GAD[, we have confirmed that genetic variants in CDKAL1 and near MTNR1B are strongly associated with GDM in Korean women.]0.125548392012IGF2BP23185811292AC
rs1470579225917073767KCNJ11umls:C0085207BeFree13 SNPs (FTO rs8050136, CDKAL1 rs7754840 and rs7756992, CDKN2A/2B rs10811661, HHEX rs1111875, IGF2BP2 rs1470579 and rs4402960, SLC30A8 rs13266634, TCF7L2 rs7903146, PPARG rs1801282, GCK rs1799884, HNF1A rs1169288, and KCNJ11 rs5219) were genotyped in 793 women with GDM after a median follow-up of 57 months.0.0091729422012IGF2BP23185811292AC
rs163184259739436934TCF7L2umls:C0085207BeFreeAssociation with GDM was found for two of the most frequently replicated T2D loci: a TCF7L2 haplotype (CTTC: rs7901695, rs4506565, rs7903146, rs12243326; P=2.16 x 10(-06); OR=2.95) and a KCNQ1 haplotype (TTT: rs2237892, rs163184, rs2237897; P=1.98 x 10(-05); OR=0.55).0.0142543932015KCNQ1112825839TG
rs1799884236903053767KCNJ11umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0091729422013GCK744189469CT
rs1799884236903054544MTNR1Bumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0021715352013GCK744189469CT
rs1799884256338832645GCKumls:C0085207BeFreeAssociation of the glucokinase gene promoter polymorphism -30G > A (rs1799884) with gestational diabetes mellitus susceptibility: a case-control study and meta-analysis.0.1448082882015GCK744189469CT
rs17998842369030554901CDKAL1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1234527992013GCK744189469CT
rs1799884236903053667IRS1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0053528932013GCK744189469CT
rs1799884225917073767KCNJ11umls:C0085207BeFree13 SNPs (FTO rs8050136, CDKAL1 rs7754840 and rs7756992, CDKN2A/2B rs10811661, HHEX rs1111875, IGF2BP2 rs1470579 and rs4402960, SLC30A8 rs13266634, TCF7L2 rs7903146, PPARG rs1801282, GCK rs1799884, HNF1A rs1169288, and KCNJ11 rs5219) were genotyped in 793 women with GDM after a median follow-up of 57 months.0.0091729422012GCK744189469CT
rs1799884236903052645GCKumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1448082882013GCK744189469CT
rs17998842369030510644IGF2BP2umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.125548392013GCK744189469CT
rs1799983244030144846NOS3umls:C0085207BeFreeThe association of endothelial nitric oxide synthase gene G894T polymorphism and serum nitric oxide concentration with microalbuminuria in patients with gestational diabetes.0.0005428842014NOS37150999023TG
rs179998324403014213ALBumls:C0085207BeFreeThe G894T polymorphism of eNOS gene and decreased NO concentration seem to be independent predictors of increased urinary excretion of albumin in patients with GDM.0.0005428842014NOS37150999023TG
rs1800629220704253586IL10umls:C0085207BeFreeOur study aimed to assess in vitro production of IL-10, IL-6, TNF-A, and adiponectin serum levels in pregnant women with and without gestational diabetes mellitus (GDM) and to investigate a possible association between GDM and IL-10-1082 A>G (rs1800896), IL-6-174 G>C (rs1800795), TNF-A-308 G>A (rs1800629), adiponectin +45 T>G (rs2241766), and adiponectin-11377 C>G (rs266729) gene polymorphisms.0.0029099162012TNF631575254GA
rs1800629220704257124TNFumls:C0085207BeFreeOur study aimed to assess in vitro production of IL-10, IL-6, TNF-A, and adiponectin serum levels in pregnant women with and without gestational diabetes mellitus (GDM) and to investigate a possible association between GDM and IL-10-1082 A>G (rs1800896), IL-6-174 G>C (rs1800795), TNF-A-308 G>A (rs1800629), adiponectin +45 T>G (rs2241766), and adiponectin-11377 C>G (rs266729) gene polymorphisms.0.0261616162012TNF631575254GA
rs1800629220704253569IL6umls:C0085207BeFreeOur study aimed to assess in vitro production of IL-10, IL-6, TNF-A, and adiponectin serum levels in pregnant women with and without gestational diabetes mellitus (GDM) and to investigate a possible association between GDM and IL-10-1082 A>G (rs1800896), IL-6-174 G>C (rs1800795), TNF-A-308 G>A (rs1800629), adiponectin +45 T>G (rs2241766), and adiponectin-11377 C>G (rs266729) gene polymorphisms.0.0008143262012TNF631575254GA
rs1800795220704253586IL10umls:C0085207BeFreeOur study aimed to assess in vitro production of IL-10, IL-6, TNF-A, and adiponectin serum levels in pregnant women with and without gestational diabetes mellitus (GDM) and to investigate a possible association between GDM and IL-10-1082 A>G (rs1800896), IL-6-174 G>C (rs1800795), TNF-A-308 G>A (rs1800629), adiponectin +45 T>G (rs2241766), and adiponectin-11377 C>G (rs266729) gene polymorphisms.0.0029099162012IL6;LOC541472722727026CG
rs1800795220704257124TNFumls:C0085207BeFreeOur study aimed to assess in vitro production of IL-10, IL-6, TNF-A, and adiponectin serum levels in pregnant women with and without gestational diabetes mellitus (GDM) and to investigate a possible association between GDM and IL-10-1082 A>G (rs1800896), IL-6-174 G>C (rs1800795), TNF-A-308 G>A (rs1800629), adiponectin +45 T>G (rs2241766), and adiponectin-11377 C>G (rs266729) gene polymorphisms.0.0261616162012IL6;LOC541472722727026CG
rs1800795220704253569IL6umls:C0085207BeFreeOur study aimed to assess in vitro production of IL-10, IL-6, TNF-A, and adiponectin serum levels in pregnant women with and without gestational diabetes mellitus (GDM) and to investigate a possible association between GDM and IL-10-1082 A>G (rs1800896), IL-6-174 G>C (rs1800795), TNF-A-308 G>A (rs1800629), adiponectin +45 T>G (rs2241766), and adiponectin-11377 C>G (rs266729) gene polymorphisms.0.0008143262012IL6;LOC541472722727026CG
rs1800896220704257124TNFumls:C0085207BeFreeOur study aimed to assess in vitro production of IL-10, IL-6, TNF-A, and adiponectin serum levels in pregnant women with and without gestational diabetes mellitus (GDM) and to investigate a possible association between GDM and IL-10-1082 A>G (rs1800896), IL-6-174 G>C (rs1800795), TNF-A-308 G>A (rs1800629), adiponectin +45 T>G (rs2241766), and adiponectin-11377 C>G (rs266729) gene polymorphisms.0.0261616162012IL101206773552TC
rs1800896220704253586IL10umls:C0085207BeFreeOur study aimed to assess in vitro production of IL-10, IL-6, TNF-A, and adiponectin serum levels in pregnant women with and without gestational diabetes mellitus (GDM) and to investigate a possible association between GDM and IL-10-1082 A>G (rs1800896), IL-6-174 G>C (rs1800795), TNF-A-308 G>A (rs1800629), adiponectin +45 T>G (rs2241766), and adiponectin-11377 C>G (rs266729) gene polymorphisms.0.0029099162012IL101206773552TC
rs1800896220704253569IL6umls:C0085207BeFreeOur study aimed to assess in vitro production of IL-10, IL-6, TNF-A, and adiponectin serum levels in pregnant women with and without gestational diabetes mellitus (GDM) and to investigate a possible association between GDM and IL-10-1082 A>G (rs1800896), IL-6-174 G>C (rs1800795), TNF-A-308 G>A (rs1800629), adiponectin +45 T>G (rs2241766), and adiponectin-11377 C>G (rs266729) gene polymorphisms.0.0008143262012IL101206773552TC
rs1801278205406706934TCF7L2umls:C0085207BeFreeThus, our data suggest that the common T2D susceptibility polymorphism of TCF7L2 (rs7903146 C/T) gene, and the G972R polymorphism of the IRS1 gene, seem to predispose to GDM in Greek women.0.0142543932011IRS12226795828CT,G,A
rs1801278163200833667IRS1umls:C0085207BeFreeAnalysis of the IRS1 G972R polymorphism showed that RR homozygosity was found exclusively in women with GDM (91.0, 8.3 and 0.7% vs 90.7, 9.3 and 0.0% for GG, GR and RR genotypes, respectively; p=0.014).0.0053528932005IRS12226795828CT,G,A
rs1801278236903053767KCNJ11umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0091729422013IRS12226795828CT,G,A
rs180127817046546155ADRB3umls:C0085207BeFreeWe studied possible relations between GDM and both insulin receptor substrate 1 (IRS-1) (Gly972Arg) and beta3-adrenergic receptor (ADRB3 Trp64Arg, beta3-AR) gene mutations, considered potential modifying factors in the etiology of type 2 diabetes mellitus.0.0031813582006IRS12226795828CT,G,A
rs1801278236903053667IRS1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0053528932013IRS12226795828CT,G,A
rs18012782369030510644IGF2BP2umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.125548392013IRS12226795828CT,G,A
rs1801278236903054544MTNR1Bumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0021715352013IRS12226795828CT,G,A
rs1801278165224273667IRS1umls:C0085207BeFreeAssociation of insulin receptor substrate-1 G972R variant with baseline characteristics of the patients with gestational diabetes mellitus.0.0053528932006IRS12226795828CT,G,A
rs1801278236903052645GCKumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1448082882013IRS12226795828CT,G,A
rs1801278205406703667IRS1umls:C0085207BeFreeThus, our data suggest that the common T2D susceptibility polymorphism of TCF7L2 (rs7903146 C/T) gene, and the G972R polymorphism of the IRS1 gene, seem to predispose to GDM in Greek women.0.0053528932011IRS12226795828CT,G,A
rs18012782369030554901CDKAL1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1234527992013IRS12226795828CT,G,A
rs180128217342473155ADRB3umls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0031813582007PPARG312351626CG
rs1801282173424739370ADIPOQumls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.2204276612007PPARG312351626CG
rs1801282173424732303FOXC2umls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0002714422007PPARG312351626CG
rs1801282181625035468PPARGumls:C0085207BeFreeWe hypothesized that interaction between PPARG2 Pro12Ala and variants in the promoter region of HNF4A are associated with type 2 diabetes-related quantitative traits in Mexican-American families of a proband with previous gestational diabetes.0.0071770412008PPARG312351626CG
rs1801282173424735468PPARGumls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0071770412007PPARG312351626CG
rs1801282225917073767KCNJ11umls:C0085207BeFree13 SNPs (FTO rs8050136, CDKAL1 rs7754840 and rs7756992, CDKN2A/2B rs10811661, HHEX rs1111875, IGF2BP2 rs1470579 and rs4402960, SLC30A8 rs13266634, TCF7L2 rs7903146, PPARG rs1801282, GCK rs1799884, HNF1A rs1169288, and KCNJ11 rs5219) were genotyped in 793 women with GDM after a median follow-up of 57 months.0.0091729422012PPARG312351626CG
rs1801282181625033172HNF4Aumls:C0085207BeFreeWe hypothesized that interaction between PPARG2 Pro12Ala and variants in the promoter region of HNF4A are associated with type 2 diabetes-related quantitative traits in Mexican-American families of a proband with previous gestational diabetes.0.0095440732008PPARG312351626CG
rs1801282230540245468PPARGumls:C0085207BeFreeQuantitative assessment of the influence of PPARG P12A polymorphism on gestational diabetes mellitus risk.0.0071770412013PPARG312351626CG
rs1801282217954475468PPARGumls:C0085207BeFreeAssociation of the Pro12Ala and C1431T variants of PPARgamma and their haplotypes with susceptibility to gestational diabetes.0.0071770412011PPARG312351626CG
rs18012821734247310891PPARGC1Aumls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0005428842007PPARG312351626CG
rs1805097244011338660IRS2umls:C0085207BeFreeThe G1057D polymorphism of insulin receptor substrate-2 associated with gestational diabetes mellitus.0.0008143262014IRS213109782884CT
rs1805192181625035468PPARGumls:C0085207BeFreeWe hypothesized that interaction between PPARG2 Pro12Ala and variants in the promoter region of HNF4A are associated with type 2 diabetes-related quantitative traits in Mexican-American families of a proband with previous gestational diabetes.0.0071770412008PPARG312379739CG
rs1805192230540245468PPARGumls:C0085207BeFreeQuantitative assessment of the influence of PPARG P12A polymorphism on gestational diabetes mellitus risk.0.0071770412013PPARG312379739CG
rs1805192173424735468PPARGumls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0071770412007PPARG312379739CG
rs1805192217954475468PPARGumls:C0085207BeFreeAssociation of the Pro12Ala and C1431T variants of PPARgamma and their haplotypes with susceptibility to gestational diabetes.0.0071770412011PPARG312379739CG
rs1805192173424739370ADIPOQumls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.2204276612007PPARG312379739CG
rs1805192173424732303FOXC2umls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0002714422007PPARG312379739CG
rs18051921734247310891PPARGC1Aumls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0005428842007PPARG312379739CG
rs1805192181625033172HNF4Aumls:C0085207BeFreeWe hypothesized that interaction between PPARG2 Pro12Ala and variants in the promoter region of HNF4A are associated with type 2 diabetes-related quantitative traits in Mexican-American families of a proband with previous gestational diabetes.0.0095440732008PPARG312379739CG
rs180519217342473155ADRB3umls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0031813582007PPARG312379739CG
rs193922331NA2645GCKumls:C0085207CLINVARNA0.144808288NAGCK;LOC105375258744147726AG
rs2021966252228395167ENPP1umls:C0085207BeFreeBody mass index associated to rs2021966 ENPP1 polymorphism increases the risk for gestational diabetes mellitus.0.0008143262015ENPP16131829299AG
rs2237892259739436934TCF7L2umls:C0085207BeFreeAssociation with GDM was found for two of the most frequently replicated T2D loci: a TCF7L2 haplotype (CTTC: rs7901695, rs4506565, rs7903146, rs12243326; P=2.16 x 10(-06); OR=2.95) and a KCNQ1 haplotype (TTT: rs2237892, rs163184, rs2237897; P=1.98 x 10(-05); OR=0.55).0.0142543932015KCNQ1112818521CT
rs2237895198506813630INSumls:C0085207BeFreeIn the analyses of the GDM-related phenotype, only the risk allele of KCNQ1 rs2237895 was significantly associated with a high-level insulin sensitivity oral glucose tolerance test among patients with GDM (P = 0.0003, 0.004, and 0.05 for codominant, dominant, and recessive models, respectively).0.0238208712010KCNQ1112835964AC
rs2237897259739436934TCF7L2umls:C0085207BeFreeAssociation with GDM was found for two of the most frequently replicated T2D loci: a TCF7L2 haplotype (CTTC: rs7901695, rs4506565, rs7903146, rs12243326; P=2.16 x 10(-06); OR=2.95) and a KCNQ1 haplotype (TTT: rs2237892, rs163184, rs2237897; P=1.98 x 10(-05); OR=0.55).0.0142543932015KCNQ1112837316CT
rs2241766220704253569IL6umls:C0085207BeFreeOur study aimed to assess in vitro production of IL-10, IL-6, TNF-A, and adiponectin serum levels in pregnant women with and without gestational diabetes mellitus (GDM) and to investigate a possible association between GDM and IL-10-1082 A>G (rs1800896), IL-6-174 G>C (rs1800795), TNF-A-308 G>A (rs1800629), adiponectin +45 T>G (rs2241766), and adiponectin-11377 C>G (rs266729) gene polymorphisms.0.0008143262012ADIPOQ;ADIPOQ-AS13186853103TG
rs2241766220704253586IL10umls:C0085207BeFreeOur study aimed to assess in vitro production of IL-10, IL-6, TNF-A, and adiponectin serum levels in pregnant women with and without gestational diabetes mellitus (GDM) and to investigate a possible association between GDM and IL-10-1082 A>G (rs1800896), IL-6-174 G>C (rs1800795), TNF-A-308 G>A (rs1800629), adiponectin +45 T>G (rs2241766), and adiponectin-11377 C>G (rs266729) gene polymorphisms.0.0029099162012ADIPOQ;ADIPOQ-AS13186853103TG
rs2241766220704257124TNFumls:C0085207BeFreeOur study aimed to assess in vitro production of IL-10, IL-6, TNF-A, and adiponectin serum levels in pregnant women with and without gestational diabetes mellitus (GDM) and to investigate a possible association between GDM and IL-10-1082 A>G (rs1800896), IL-6-174 G>C (rs1800795), TNF-A-308 G>A (rs1800629), adiponectin +45 T>G (rs2241766), and adiponectin-11377 C>G (rs266729) gene polymorphisms.0.0261616162012ADIPOQ;ADIPOQ-AS13186853103TG
rs2383208220965103630INSumls:C0085207BeFreeWe also found that the risk alleles of rs2383208 (b = -0.085, p = 0.003), rs4402960 (b = -0.057, p = 0.046) and rs10830963 (b = -0.096, p = 0.001) were associated with HOMA-B, while rs7754840 was associated with decrease in insulin AUC during a 100 g OGTT given at the time of GDM diagnosis (b = -0.080, p = 0.007).0.0238208712011NA922132077AG,T
rs266729240682959370ADIPOQumls:C0085207BeFreeThe rs266729 single-nucleotide polymorphism in the adiponectin gene shows association with gestational diabetes.0.2204276612013ADIPOQ3186841685CG
rs266729220704253569IL6umls:C0085207BeFreeOur study aimed to assess in vitro production of IL-10, IL-6, TNF-A, and adiponectin serum levels in pregnant women with and without gestational diabetes mellitus (GDM) and to investigate a possible association between GDM and IL-10-1082 A>G (rs1800896), IL-6-174 G>C (rs1800795), TNF-A-308 G>A (rs1800629), adiponectin +45 T>G (rs2241766), and adiponectin-11377 C>G (rs266729) gene polymorphisms.0.0008143262012ADIPOQ3186841685CG
rs266729220704253586IL10umls:C0085207BeFreeOur study aimed to assess in vitro production of IL-10, IL-6, TNF-A, and adiponectin serum levels in pregnant women with and without gestational diabetes mellitus (GDM) and to investigate a possible association between GDM and IL-10-1082 A>G (rs1800896), IL-6-174 G>C (rs1800795), TNF-A-308 G>A (rs1800629), adiponectin +45 T>G (rs2241766), and adiponectin-11377 C>G (rs266729) gene polymorphisms.0.0029099162012ADIPOQ3186841685CG
rs266729220704257124TNFumls:C0085207BeFreeOur study aimed to assess in vitro production of IL-10, IL-6, TNF-A, and adiponectin serum levels in pregnant women with and without gestational diabetes mellitus (GDM) and to investigate a possible association between GDM and IL-10-1082 A>G (rs1800896), IL-6-174 G>C (rs1800795), TNF-A-308 G>A (rs1800629), adiponectin +45 T>G (rs2241766), and adiponectin-11377 C>G (rs266729) gene polymorphisms.0.0261616162012ADIPOQ3186841685CG
rs2796441237614236934TCF7L2umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0142543932013LOC101927502981694033GA
rs279644123761423111ADCY5umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013LOC101927502981694033GA
rs2796441237614232646GCKRumls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013LOC101927502981694033GA
rs2796441237614237088TLE1umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013LOC101927502981694033GA
rs27964412376142357818G6PC2umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013LOC101927502981694033GA
rs27964412376142379068FTOumls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0005428842013LOC101927502981694033GA
rs3856806217954475468PPARGumls:C0085207BeFreeAssociation of the Pro12Ala and C1431T variants of PPARgamma and their haplotypes with susceptibility to gestational diabetes.0.0071770412011PPARG312434058CT
rs3865979972369030554901CDKAL1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1234527992013NANANANANA
rs3865979972369030510644IGF2BP2umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.125548392013NANANANANA
rs386597997236903052645GCKumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1448082882013NANANANANA
rs386597997236903053767KCNJ11umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0091729422013NANANANANA
rs386597997163200833767KCNJ11umls:C0085207BeFreeAssociation of the E23K polymorphism in the KCNJ11 gene with gestational diabetes mellitus.0.0091729422005NANANANANA
rs386597997236903054544MTNR1Bumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0021715352013NANANANANA
rs386597997236903053667IRS1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0053528932013NANANANANA
rs4402960220965103630INSumls:C0085207BeFreeWe also found that the risk alleles of rs2383208 (b = -0.085, p = 0.003), rs4402960 (b = -0.057, p = 0.046) and rs10830963 (b = -0.096, p = 0.001) were associated with HOMA-B, while rs7754840 was associated with decrease in insulin AUC during a 100 g OGTT given at the time of GDM diagnosis (b = -0.080, p = 0.007).0.0238208712011IGF2BP23185793899GT
rs44029602369030510644IGF2BP2umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.125548392013IGF2BP23185793899GT
rs44029602369030554901CDKAL1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1234527992013IGF2BP23185793899GT
rs4402960236903053767KCNJ11umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0091729422013IGF2BP23185793899GT
rs4402960236903054544MTNR1Bumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0021715352013IGF2BP23185793899GT
rs4402960236903053667IRS1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0053528932013IGF2BP23185793899GT
rs4402960225917073767KCNJ11umls:C0085207BeFree13 SNPs (FTO rs8050136, CDKAL1 rs7754840 and rs7756992, CDKN2A/2B rs10811661, HHEX rs1111875, IGF2BP2 rs1470579 and rs4402960, SLC30A8 rs13266634, TCF7L2 rs7903146, PPARG rs1801282, GCK rs1799884, HNF1A rs1169288, and KCNJ11 rs5219) were genotyped in 793 women with GDM after a median follow-up of 57 months.0.0091729422012IGF2BP23185793899GT
rs4402960236903052645GCKumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1448082882013IGF2BP23185793899GT
rs4506565259739436934TCF7L2umls:C0085207BeFreeAssociation with GDM was found for two of the most frequently replicated T2D loci: a TCF7L2 haplotype (CTTC: rs7901695, rs4506565, rs7903146, rs12243326; P=2.16 x 10(-06); OR=2.95) and a KCNQ1 haplotype (TTT: rs2237892, rs163184, rs2237897; P=1.98 x 10(-05); OR=0.55).0.0142543932015TCF7L210112996282AT
rs499417046546155ADRB3umls:C0085207BeFreeWe studied possible relations between GDM and both insulin receptor substrate 1 (IRS-1) (Gly972Arg) and beta3-adrenergic receptor (ADRB3 Trp64Arg, beta3-AR) gene mutations, considered potential modifying factors in the etiology of type 2 diabetes mellitus.0.0031813582006ADRB3837966280AG
rs4994173424735468PPARGumls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0071770412007ADRB3837966280AG
rs499417342473155ADRB3umls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0031813582007ADRB3837966280AG
rs499415334374155ADRB3umls:C0085207BeFreeOur results indicated that the ADRB3 Trp64Arg variant is not related to the development of GDM and has no effect on obesity during pregnancy in a Taiwanese population.0.0031813582004ADRB3837966280AG
rs49941734247310891PPARGC1Aumls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0005428842007ADRB3837966280AG
rs4994173424732303FOXC2umls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0002714422007ADRB3837966280AG
rs4994173424739370ADIPOQumls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.2204276612007ADRB3837966280AG
rs5015480190024303630INSumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0238208712009NA1092705802CT
rs5015480190024301029CDKN2Aumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009NA1092705802CT
rs50154801900243054901CDKAL1umls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.1234527992009NA1092705802CT
rs5015480190024301030CDKN2Bumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009NA1092705802CT
rs5015480190024303087HHEXumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009NA1092705802CT
rs5219236903053767KCNJ11umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0091729422013KCNJ111117388025TC
rs5219236903053667IRS1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0053528932013KCNJ111117388025TC
rs5219236903052645GCKumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1448082882013KCNJ111117388025TC
rs5219163200833767KCNJ11umls:C0085207BeFreeAssociation of the E23K polymorphism in the KCNJ11 gene with gestational diabetes mellitus.0.0091729422005KCNJ111117388025TC
rs5219225917073767KCNJ11umls:C0085207BeFree13 SNPs (FTO rs8050136, CDKAL1 rs7754840 and rs7756992, CDKN2A/2B rs10811661, HHEX rs1111875, IGF2BP2 rs1470579 and rs4402960, SLC30A8 rs13266634, TCF7L2 rs7903146, PPARG rs1801282, GCK rs1799884, HNF1A rs1169288, and KCNJ11 rs5219) were genotyped in 793 women with GDM after a median follow-up of 57 months.0.0091729422012KCNJ111117388025TC
rs52192369030510644IGF2BP2umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.125548392013KCNJ111117388025TC
rs5219236903054544MTNR1Bumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0021715352013KCNJ111117388025TC
rs52192369030554901CDKAL1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1234527992013KCNJ111117388025TC
rs56088723761423111ADCY5umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013G6PC22168906638TC
rs560887237614236934TCF7L2umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0142543932013G6PC22168906638TC
rs5608872376142379068FTOumls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0005428842013G6PC22168906638TC
rs560887237614237088TLE1umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013G6PC22168906638TC
rs560887237614232646GCKRumls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013G6PC22168906638TC
rs5608872376142357818G6PC2umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013G6PC22168906638TC
rs587780343NA2645GCKumls:C0085207CLINVARNA0.144808288NAGCK744145638CA
rs587780345NA2645GCKumls:C0085207CLINVARNA0.144808288NAGCK;LOC105375258744150004CT
rs587780346NA2645GCKumls:C0085207CLINVARNA0.144808288NAGCK;LOC105375258744149823TG
rs587780347NA2645GCKumls:C0085207CLINVARNA0.144808288NAGCK;LOC105375258744147807CT
rs662250368965444PON1umls:C0085207BeFreeRelationship between the paraoxonase 1 gene glutamine 192 to arginine polymorphism and gestational diabetes mellitus in Saudi women.0.0002714422014PON1795308134TC
rs7384092564632880339PNPLA3umls:C0085207BeFreeIsoleucine-to-methionine substitution at residue 148 variant of PNPLA3 gene and metabolic outcomes in gestational diabetes.0.0002714422015PNPLA32243928847CG
rs7754840220965103630INSumls:C0085207BeFreeWe also found that the risk alleles of rs2383208 (b = -0.085, p = 0.003), rs4402960 (b = -0.057, p = 0.046) and rs10830963 (b = -0.096, p = 0.001) were associated with HOMA-B, while rs7754840 was associated with decrease in insulin AUC during a 100 g OGTT given at the time of GDM diagnosis (b = -0.080, p = 0.007).0.0238208712011CDKAL1620661019GC,T
rs77548402223365154901CDKAL1umls:C0085207GWASCATIn conclusion, we have confirmed that genetic variants in CDKAL1 and near MTNR1B are strongly associated with GDM in Korean women.0.1234527992012CDKAL1620661019GC,T
rs7754840190024301029CDKN2Aumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009CDKAL1620661019GC,T
rs7754840236903053667IRS1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0053528932013CDKAL1620661019GC,T
rs7754840225917073767KCNJ11umls:C0085207BeFree13 SNPs (FTO rs8050136, CDKAL1 rs7754840 and rs7756992, CDKN2A/2B rs10811661, HHEX rs1111875, IGF2BP2 rs1470579 and rs4402960, SLC30A8 rs13266634, TCF7L2 rs7903146, PPARG rs1801282, GCK rs1799884, HNF1A rs1169288, and KCNJ11 rs5219) were genotyped in 793 women with GDM after a median follow-up of 57 months.0.0091729422012CDKAL1620661019GC,T
rs77548402369030554901CDKAL1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1234527992013CDKAL1620661019GC,T
rs7754840190024303630INSumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0238208712009CDKAL1620661019GC,T
rs7754840236903054544MTNR1Bumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0021715352013CDKAL1620661019GC,T
rs77548401900243054901CDKAL1umls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.1234527992009CDKAL1620661019GC,T
rs77548402223365154901CDKAL1umls:C0085207GAD[In conclusion, we have confirmed that genetic variants in CDKAL1 and near MTNR1B are strongly associated with GDM in Korean women.]0.1234527992012CDKAL1620661019GC,T
rs7754840190024303087HHEXumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009CDKAL1620661019GC,T
rs7754840236903052645GCKumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1448082882013CDKAL1620661019GC,T
rs7754840236903053767KCNJ11umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0091729422013CDKAL1620661019GC,T
rs7754840190024301030CDKN2Bumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009CDKAL1620661019GC,T
rs77548402369030510644IGF2BP2umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.125548392013CDKAL1620661019GC,T
rs7756992190024301030CDKN2Bumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009CDKAL1620679478AG
rs77569921900243054901CDKAL1umls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.1234527992009CDKAL1620679478AG
rs7756992225917073767KCNJ11umls:C0085207BeFree13 SNPs (FTO rs8050136, CDKAL1 rs7754840 and rs7756992, CDKN2A/2B rs10811661, HHEX rs1111875, IGF2BP2 rs1470579 and rs4402960, SLC30A8 rs13266634, TCF7L2 rs7903146, PPARG rs1801282, GCK rs1799884, HNF1A rs1169288, and KCNJ11 rs5219) were genotyped in 793 women with GDM after a median follow-up of 57 months.0.0091729422012CDKAL1620679478AG
rs7756992190024301029CDKN2Aumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009CDKAL1620679478AG
rs7756992190024303630INSumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0238208712009CDKAL1620679478AG
rs7756992190024303087HHEXumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009CDKAL1620679478AG
rs78009423761423111ADCY5umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013GCKR227518370TC
rs7800942376142379068FTOumls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0005428842013GCKR227518370TC
rs780094237614237088TLE1umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013GCKR227518370TC
rs7800942376142357818G6PC2umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013GCKR227518370TC
rs780094234569076934TCF7L2umls:C0085207BeFreeAmong Caucasian women, GDM was associated with carriage of TCF7L2 rs7901695, MTNR1B rs10830963 and GCKR rs780094 alleles that are associated with T2DM and fasting glucose in nonpregnant populations.0.0142543932014GCKR227518370TC
rs780094237614236934TCF7L2umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0142543932013GCKR227518370TC
rs780094237614232646GCKRumls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013GCKR227518370TC
rs7901695234569076934TCF7L2umls:C0085207BeFreeAmong Caucasian women, GDM was associated with carriage of TCF7L2 rs7901695, MTNR1B rs10830963 and GCKR rs780094 alleles that are associated with T2DM and fasting glucose in nonpregnant populations.0.0142543932014TCF7L210112994329TC
rs7901695259739436934TCF7L2umls:C0085207BeFreeAssociation with GDM was found for two of the most frequently replicated T2D loci: a TCF7L2 haplotype (CTTC: rs7901695, rs4506565, rs7903146, rs12243326; P=2.16 x 10(-06); OR=2.95) and a KCNQ1 haplotype (TTT: rs2237892, rs163184, rs2237897; P=1.98 x 10(-05); OR=0.55).0.0142543932015TCF7L210112994329TC
rs7903146237614232646GCKRumls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013TCF7L210112998590CT
rs7903146259739436934TCF7L2umls:C0085207BeFreeAssociation with GDM was found for two of the most frequently replicated T2D loci: a TCF7L2 haplotype (CTTC: rs7901695, rs4506565, rs7903146, rs12243326; P=2.16 x 10(-06); OR=2.95) and a KCNQ1 haplotype (TTT: rs2237892, rs163184, rs2237897; P=1.98 x 10(-05); OR=0.55).0.0142543932015TCF7L210112998590CT
rs790314623761423111ADCY5umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013TCF7L210112998590CT
rs79031462376142357818G6PC2umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013TCF7L210112998590CT
rs79031462259170779068FTOumls:C0085207BeFreeThe TCF7L2 rs7903146 and FTO rs8050136 polymorphisms, and particularly a weighted risk score of T2D risk alleles, predict diabetes after GDM.0.0005428842012TCF7L210112998590CT
rs7903146236903053667IRS1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0053528932013TCF7L210112998590CT
rs7903146205406706934TCF7L2umls:C0085207BeFreeThus, our data suggest that the common T2D susceptibility polymorphism of TCF7L2 (rs7903146 C/T) gene, and the G972R polymorphism of the IRS1 gene, seem to predispose to GDM in Greek women.0.0142543932011TCF7L210112998590CT
rs7903146225917073767KCNJ11umls:C0085207BeFree13 SNPs (FTO rs8050136, CDKAL1 rs7754840 and rs7756992, CDKN2A/2B rs10811661, HHEX rs1111875, IGF2BP2 rs1470579 and rs4402960, SLC30A8 rs13266634, TCF7L2 rs7903146, PPARG rs1801282, GCK rs1799884, HNF1A rs1169288, and KCNJ11 rs5219) were genotyped in 793 women with GDM after a median follow-up of 57 months.0.0091729422012TCF7L210112998590CT
rs79031462369030554901CDKAL1umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1234527992013TCF7L210112998590CT
rs7903146236903052645GCKumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.1448082882013TCF7L210112998590CT
rs79031462376142379068FTOumls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0005428842013TCF7L210112998590CT
rs7903146237614237088TLE1umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013TCF7L210112998590CT
rs7903146236903054544MTNR1Bumls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0021715352013TCF7L210112998590CT
rs7903146236903056934TCF7L2umls:C0085207BeFreeAmong them, genetic variants in TCF7L2 showed the strongest association with GDM risk, with ORs (95% CIs) of 1.44 (1.29-1.60, P < 0.001) per T allele of rs7903146 and 1.46 (1.15-1.84, P = 0.002) per T allele of rs12255372.0.0142543932013TCF7L210112998590CT
rs7903146238553526934TCF7L2umls:C0085207BeFreeAssociation of the rs7903146 polymorphism in transcription factor 7-like 2 (TCF7L2) gene with gestational diabetes mellitus: a meta-analysis.0.0142543932014TCF7L210112998590CT
rs7903146236903053767KCNJ11umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.0091729422013TCF7L210112998590CT
rs7903146237614236934TCF7L2umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0142543932013TCF7L210112998590CT
rs79031462369030510644IGF2BP2umls:C0085207BeFreeThe minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM.0.125548392013TCF7L210112998590CT
rs7903146205406703667IRS1umls:C0085207BeFreeThus, our data suggest that the common T2D susceptibility polymorphism of TCF7L2 (rs7903146 C/T) gene, and the G972R polymorphism of the IRS1 gene, seem to predispose to GDM in Greek women.0.0053528932011TCF7L210112998590CT
rs7923837190024301030CDKN2Bumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009NA1092722160GA
rs7923837190024301029CDKN2Aumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009NA1092722160GA
rs7923837190024303630INSumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0238208712009NA1092722160GA
rs79238371900243054901CDKAL1umls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.1234527992009NA1092722160GA
rs7923837190024303087HHEXumls:C0085207BeFreeThe risk alleles of the SNPs rs7756992 and rs7754840 in CDKAL1; rs10811661 in the CDKN2A-CDKN2B region; and rs1111875, rs5015480 and rs7923837 in HHEX were associated with significant decreases in the insulin AUC during a 100 g OGTT performed at the time of diagnosis of GDM.0.0002714422009NA1092722160GA
rs8050136225917073767KCNJ11umls:C0085207BeFree13 SNPs (FTO rs8050136, CDKAL1 rs7754840 and rs7756992, CDKN2A/2B rs10811661, HHEX rs1111875, IGF2BP2 rs1470579 and rs4402960, SLC30A8 rs13266634, TCF7L2 rs7903146, PPARG rs1801282, GCK rs1799884, HNF1A rs1169288, and KCNJ11 rs5219) were genotyped in 793 women with GDM after a median follow-up of 57 months.0.0091729422012FTO1653782363CA
rs80501362259170779068FTOumls:C0085207BeFreeThe TCF7L2 rs7903146 and FTO rs8050136 polymorphisms, and particularly a weighted risk score of T2D risk alleles, predict diabetes after GDM.0.0005428842012FTO1653782363CA
rs8111699237063356794STK11umls:C0085207BeFreeIn pregnant women, the G allele for the rs8111699 variant in STK11 is associated with a more favorable metabolic phenotype and may protect against the development of GDM, particularly in heavier women.0.0002714422013STK11191209715CG
rs8192678173424732303FOXC2umls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0002714422007PPARGC1A423814039CT
rs8192678173424735468PPARGumls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0071770412007PPARGC1A423814039CT
rs81926781734247310891PPARGC1Aumls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0005428842007PPARGC1A423814039CT
rs819267817342473155ADRB3umls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.0031813582007PPARGC1A423814039CT
rs8192678173424739370ADIPOQumls:C0085207BeFreeThe other polymorphisms studied were not significantly associated with gestational diabetes mellitus (ADIPOQ +276G > T: 1.17 [1.01-1.36], p = 0.039 [Pc = 0.23]; PPARG Pro12Ala: 1.06 [0.87-1.29], p = 0.53; PPARGC1A Gly482Ser: 0.96 [0.83-1.10], p = 0.54; FOXC2 -512C > T: 1.01 [0.87-1.16], p = 0.94; and ADRB3 Trp64Arg: 1.22 [0.95-1.56], p = 0.12).0.2204276612007PPARGC1A423814039CT
rs9939609237614237088TLE1umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013FTO1653786615TA
rs99396092376142357818G6PC2umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013FTO1653786615TA
rs9939609237614232646GCKRumls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013FTO1653786615TA
rs99396092376142379068FTOumls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0005428842013FTO1653786615TA
rs9939609237614236934TCF7L2umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0142543932013FTO1653786615TA
rs993960923761423111ADCY5umls:C0085207BeFreeAdditionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).0.0002714422013FTO1653786615TA
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:47)
CHR POS SNPID REF ALT ORI_SNPID PMID P_VALUE P_VALUE_TEXT OR/BETA CI95_TEXT GWAS_INITIAL_SAMPLE_SIZE SUB_POPULATION SUPER_POPULATION GWAS_TRAIT HPO_ID HPO_TERM DO_ID DO_TERM MESH_ID MESH_TERM EFO_ID EFO_TERM DOLITE_TERM RISK_ALLELE PUBLICATION_TYPE AA GENE_SYMBOL TYPE REFGENE
15782769rs2649086TCrs2649086222336518.96E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tGNA
118722737rs1336131GTrs1336131222336515.74E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tGNA
165135341rs7513574GTrs7513574222336511.75E-06NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tGCACHD1
192177062rs17512269CTrs17512269222336515.82E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tTTGFBR3
241535003rs13415944GCrs13415944222336512.89E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCNA
2199753674rs12614240CTrs12614240222336512.40E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCNA
326775763rs1386886CTrs1386886222336512.14E-06NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tANA
326778370rs9866020GArs9866020222336515.27E-06NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tANA
326843377rs1155107AGrs1155107222336516.37E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tNANA
326847785rs9848111AGrs9848111222336512.47E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tGNA
335794900rs9865772CTrs9865772222336516.13E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tTARPP21
366868609rs10049466CTrs10049466222336519.66E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tTNA
3171270483rs360457GTrs360457222336513.02E-06NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tGNA
3185497635rs4376068ACrs4376068222336516.37E-06NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCIGF2BP2
3185499057rs6801848CGrs6801848222336511.00E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCIGF2BP2
3185511687rs4402960GTrs4402960222336517.72E-06NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tGIGF2BP2
3185513392rs7651090AGrs7651090222336512.47E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tGIGF2BP2
3185529080rs1470579ACrs1470579222336512.00E-07NA1.33[1.20-1.48] 468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesrs1470579-CResearch Support, Non-U.S. Gov'tCIGF2BP2
5173160684rs10071956TCrs10071956222336515.92E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tTNA
5173165659rs4868311TCrs4868311222336515.08E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tTNA
5173753469rs2913472CArs2913472222336512.89E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tANA
620570039rs4291090CTrs4291090222336515.01E-06NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCCDKAL1
620599628rs9366357CTrs9366357222336512.96E-06NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCCDKAL1
620599888rs2294809CTrs2294809222336511.90E-06NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tGCDKAL1
620639604rs7758612GArs7758612222336511.32E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tACDKAL1
620641336rs9348440CTrs9348440222336514.01E-10NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCCDKAL1
620659806rs6456368TCrs6456368222336513.46E-11NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCCDKAL1
620661034rs10946398ACrs10946398222336511.76E-10NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCCDKAL1
620661250rs7754840GCrs7754840222336517.00E-16NA1.52[1.37-1.68]468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesrs7754840-CResearch Support, Non-U.S. Gov'tGCDKAL1
620717255rs9465871TCrs9465871222336511.14E-07NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tTCDKAL1
620718240rs2328549ATrs2328549222336514.78E-08NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tACDKAL1
620725240rs7767391TCrs7767391222336518.25E-09NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tTCDKAL1
654247467rs1508635ACrs1508635222336512.73E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tGTINAG
973164637rs2277188CTrs2277188222336515.06E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCTRPM3
9119392413rs1885245GCrs1885245222336518.61E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCASTN2
1063613870rs10821926TCrs10821926222336515.30E-06NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tTNA
1068125841rs7914106TGrs7914106222336519.59E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tTCTNNA3
1162237317rs2513044AGrs2513044222336515.69E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCAHNAK
1192698427rs10830962CGrs10830962222336512.00E-13NA1.45[1.31-1.61]468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesrs10830962-GResearch Support, Non-U.S. Gov'tGNA
1394209956rs9524131TCrs9524131222336512.66E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCGPC6
13110995528rs9559772CGrs9559772222336514.14E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCCOL4A2
1499858970rs1257267CArs1257267222336518.55E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tTNA
1568128117rs12898654CGrs12898654222336514.37E-06NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tGNA
1671207879rs9939485GCrs9939485222336513.55E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCHYDIN
1687957458rs7499404TCrs7499404222336518.88E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tTCA5A
192242829rs7249235ACrs7249235222336518.55E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tCSF3A2
2044401404rs800684CGrs800684222336519.62E-05NANANA468 cases of Korean ancestry; 1,242 controls of Korean ancestryKorean(1710)ALL(1710)ASN(1710)ALL(1710)Diabetes (gestational)HPOID:0009800Maternal diabetesDOID:11714gestational diabetesD016640Diabetes, GestationalEFOID:0004593gestational diabetesGestational diabetesNAResearch Support, Non-U.S. Gov'tGNA
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:3)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0085207glutathioneD00597870-18-8diabetes, gestationalMESH:D016640marker/mechanism23956348
C0085207metforminD008687657-24-9diabetes, gestationalMESH:D016640therapeutic23457588
C0085207prochlorperazineD01134658-38-8diabetes, gestationalMESH:D016640marker/mechanism18480684
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)