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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   polycystic ovary syndrome
  

Disease ID 41
Disease polycystic ovary syndrome
Definition
A complex disorder characterized by infertility, HIRSUTISM; OBESITY; and various menstrual disturbances such as OLIGOMENORRHEA; AMENORRHEA; ANOVULATION. Polycystic ovary syndrome is usually associated with bilateral enlarged ovaries studded with atretic follicles, not with cysts. The term, polycystic ovary, is misleading.
Synonym
(polycystic ovaries) or (stein-leventhal syndrome)
(polycystic ovaries) or (stein-leventhal syndrome) (disorder)
bilateral polycystic ovarian syndrome
cystic disease of ovaries
disease ovarian polycystic
disease ovary polycystic
diseases ovary polycystic
hyperthecosis, ovarian
multicystic ovaries
multicystic ovaries (disorder)
ovarian degeneration, sclerocystic
ovarian hyperthecosis
ovarian polycystic disease
ovarian syndrome, polycystic
ovaries polycystic
ovary polycystic
ovary syndrome, polycystic
pco
pco - polycystic ovaries
pco1
pcod - polycystic ovarian disease
pcos
pcos - polycystic ovarian syndrome
pcos1
polycystic ovarian disease
polycystic ovarian syndrome
polycystic ovaries
polycystic ovaries (disorder)
polycystic ovary
polycystic ovary disease
polycystic ovary disorder
polycystic ovary syndrome (disorder)
polycystic ovary syndrome (pcos)
polycystic ovary syndrome 1
polycystic ovary syndrome [disease/finding]
poycystic ovarian syndrome
sclerocystic ovarian degeneration
sclerocystic ovarian disease
sclerocystic ovary syndrome
stein - leventhal syndrome
stein lenventhal syndrome
stein leventhal syndrome
stein-leventhal synd.
stein-leventhal syndrome
syndrome, polycystic ovary
syndrome, stein-leventhal
OMIM
DOID
ICD10
UMLS
C0032460
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:120)
C0021359  |  infertile  |  96
C0206081  |  hyperandrogenism  |  72
C0028754  |  obesity  |  61
C0021359  |  infertility  |  59
C0948265  |  metabolic syndrome  |  47
C0003128  |  anovulation  |  30
C0011847  |  diabetes  |  21
C0042373  |  vascular disease  |  17
C0007222  |  cardiovascular disease  |  17
C0020459  |  hyperinsulinemia  |  16
C0011849  |  diabetes mellitus  |  16
C0020538  |  hypertension  |  14
C0011570  |  depression  |  14
C0002453  |  amenorrhea  |  9
C0085207  |  gestational diabetes  |  8
C0023895  |  liver disease  |  7
C0235461  |  androgen excess  |  7
C0085207  |  gestational diabetes mellitus  |  7
C0042870  |  vitamin d defic  |  6
C0020676  |  hypothyroidism  |  6
C0159069  |  impaired glucose tolerance  |  6
C0021364  |  male infertility  |  6
C0003467  |  anxiety  |  5
C0011860  |  type 2 diabetes mellitus  |  5
C0032460  |  polycystic ovaries  |  5
C0849777  |  cystic ovaries  |  5
C0011860  |  type 2 diabetes  |  5
C0042870  |  vitamin d deficiency  |  4
C0000786  |  miscarriage  |  4
C0085083  |  ovarian hyperstimulation syndrome  |  4
C0032914  |  preeclampsia  |  4
C0040147  |  thyroiditis  |  4
C0271650  |  glucose intolerance  |  4
C0020514  |  hyperprolactinemia  |  3
C0006142  |  breast cancer  |  3
C0011854  |  type 1 diabetes  |  3
C0271650  |  prediabetes  |  3
C0154208  |  ovarian dysfunction  |  3
C0014130  |  endocrine disorders  |  3
C0033953  |  sexual dysfunction  |  3
C0476089  |  endometrial ca  |  3
C1140680  |  ovarian ca  |  2
C0004936  |  mental disorders  |  2
C0852949  |  arterial disease  |  2
C0033845  |  idiopathic intracranial hypertension  |  2
C0028754  |  adiposity  |  2
C0023787  |  lipodystrophy  |  2
C0005586  |  bipolar disorder  |  2
C0011854  |  type 1 diabetes mellitus  |  2
C0001144  |  acne vulgaris  |  2
C0476089  |  endometrial cancer  |  2
C0920350  |  autoimmune thyroiditis  |  2
C0151740  |  intracranial hypertension  |  2
C0520679  |  obstructive sleep apnea  |  2
C0020459  |  hyperinsulinaemia  |  2
C0014130  |  hormonal imbalance  |  2
C0013537  |  eclampsia  |  2
C0018021  |  goiter  |  2
C0004153  |  atherosclerosis  |  2
C0020676  |  hypothyroid  |  2
C0032460  |  polycystic ovary  |  2
C0000809  |  recurrent miscarriage  |  2
C0000786  |  spontaneous abortion  |  2
C1140680  |  ovarian cancer  |  1
C0021053  |  immune disorder  |  1
C0035579  |  hypovitaminosis d  |  1
C0282193  |  iron overload  |  1
C0008029  |  cherubism  |  1
C0014130  |  endocrine disease  |  1
C0017920  |  glycogen storage disease type i  |  1
C0040128  |  thyroid disorders  |  1
C0020459  |  hyperinsulinism  |  1
C0037317  |  sleep disturbances  |  1
C0020555  |  hypertrichosis  |  1
C0014544  |  epilepsy  |  1
C0002453  |  amenorrhoea  |  1
C0033860  |  psoriasis  |  1
C0021655  |  insulin resistance syndrome  |  1
C0010068  |  coronary artery disease  |  1
C0020619  |  hypogonadism  |  1
C0037317  |  sleep disturbance  |  1
C0851578  |  sleep disorders  |  1
C0677607  |  hashimoto's thyroiditis  |  1
C0030319  |  panic disorder  |  1
C0040128  |  thyroid disease  |  1
C0029927  |  ovarian cysts  |  1
C0014130  |  endocrine disturbance  |  1
C0029927  |  ovarian cyst  |  1
C0006370  |  bulimia  |  1
C0398623  |  thrombophilia  |  1
C0000809  |  recurrent miscarriages  |  1
C0242520  |  chronic thyroiditis  |  1
C0028756  |  morbid obesity  |  1
C0270549  |  generalized anxiety disorder  |  1
C0041696  |  major depression  |  1
C0033975  |  psychosis  |  1
C0002170  |  alopecia  |  1
C0836924  |  thrombocytosis  |  1
C0032460  |  polycystic ovary syndrome  |  1
C0023267  |  leiomyomas  |  1
C0042170  |  vogt-koyanagi-harada disease  |  1
C0021053  |  immune disorders  |  1
C0031090  |  periodontal disease  |  1
C0034013  |  precocious puberty  |  1
C0042170  |  harada disease  |  1
C0476089  |  endometrial carcinoma  |  1
C0007222  |  cardiovascular diseases  |  1
C0034013  |  early puberty  |  1
C0018213  |  graves' disease  |  1
C0003469  |  anxiety disorder  |  1
C0001430  |  adenoma  |  1
C0000786  |  spontaneous abortions  |  1
C0497327  |  dementia  |  1
C1621895  |  adrenal hyperplasia  |  1
C0037315  |  sleep apnea  |  1
C0042373  |  vascular diseases  |  1
C0017919  |  glycogen storage disease  |  1
C0017075  |  ganglioneuroma  |  1
C0398625  |  protein c deficiency  |  1
C1510471  |  hypovitaminosis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:152)
3972  |  LHB  |  CTD_human
3630  |  INS  |  CTD_human
8091  |  HMGA2  |  GWASCAT
2778  |  GNAS  |  CTD_human
10468  |  FST  |  CTD_human
79039  |  DDX54  |  CTD_human
54206  |  ERRFI1  |  CTD_human
57104  |  PNPLA2  |  CTD_human
55783  |  CMTR2  |  CTD_human
116840  |  CNTROB  |  CTD_human
2661  |  GDF9  |  CTD_human
6168  |  RPL37A  |  CTD_human
5724  |  PTAFR  |  CTD_human
2324  |  FLT4  |  CTD_human
10058  |  ABCB6  |  CTD_human
6899  |  TBX1  |  CTD_human
1164  |  CKS2  |  CTD_human
2492  |  FSHR  |  CTD_human;GWASCAT
596  |  BCL2  |  CTD_human
4058  |  LTK  |  CTD_human
6337  |  SCNN1A  |  CTD_human
259266  |  ASPM  |  CTD_human
3161  |  HMMR  |  CTD_human
1756  |  DMD  |  CTD_human
1588  |  CYP19A1  |  CTD_human
6241  |  RRM2  |  CTD_human
63892  |  THADA  |  GWASCAT
164395  |  TTLL9  |  CTD_human
3643  |  INSR  |  GWASCAT
891  |  CCNB1  |  CTD_human
6102  |  RP2  |  CTD_human
3070  |  HELLS  |  CTD_human
144577  |  C12orf66  |  CTD_human
23658  |  LSM5  |  CTD_human
7153  |  TOP2A  |  CTD_human
4000  |  LMNA  |  CTD_human
50943  |  FOXP3  |  CTD_human
6821  |  SUOX  |  GWASCAT
7037  |  TFRC  |  CTD_human
9210  |  BMP15  |  CTD_human
57449  |  PLEKHG5  |  CTD_human
817  |  CAMK2D  |  CTD_human
3977  |  LIFR  |  CTD_human
9205  |  ZMYM5  |  CTD_human
4085  |  MAD2L1  |  CTD_human
1742  |  DLG4  |  CTD_human
79685  |  SAP30L  |  CTD_human
6286  |  S100P  |  CTD_human
53335  |  BCL11A  |  CTD_human
581  |  BAX  |  CTD_human
864  |  RUNX3  |  CTD_human
5869  |  RAB5B  |  GWASCAT
653545  |  DUX4L5  |  CTD_human
3084  |  NRG1  |  CTD_human
25865  |  PRKD2  |  CTD_human
338324  |  S100A7A  |  CTD_human
2812  |  GP1BB  |  CTD_human
6440  |  SFTPC  |  CTD_human
5733  |  PTGER3  |  CTD_human
440836  |  ODF3B  |  CTD_human
990  |  CDC6  |  CTD_human
3500  |  IGHG1  |  CTD_human
8644  |  AKR1C3  |  CTD_human
3973  |  LHCGR  |  GWASCAT
55872  |  PBK  |  CTD_human
55721  |  IQCC  |  CTD_human
10413  |  YAP1  |  GWASCAT
257106  |  ARHGAP30  |  CTD_human
171558  |  PTCRA  |  CTD_human
3284  |  HSD3B2  |  CTD_human
93611  |  FBXO44  |  CTD_human
6665  |  SOX15  |  CTD_human
90326  |  THAP3  |  CTD_human
131566  |  DCBLD2  |  CTD_human
29127  |  RACGAP1  |  CTD_human
6770  |  STAR  |  CTD_human
10772  |  SRSF10  |  CTD_human
79694  |  MANEA  |  CTD_human
80264  |  ZNF430  |  CTD_human
3850  |  KRT3  |  CTD_human
6715  |  SRD5A1  |  CTD_human
8463  |  TEAD2  |  CTD_human
29997  |  GLTSCR2  |  CTD_human
23671  |  TMEFF2  |  CTD_human
55165  |  CEP55  |  CTD_human
286749  |  STON1-GTF2A1L  |  GWASCAT
146664  |  MGAT5B  |  CTD_human
51477  |  ISYNA1  |  CTD_human
5950  |  RBP4  |  CTD_human
8572  |  PDLIM4  |  CTD_human
1013  |  CDH15  |  CTD_human
3952  |  LEP  |  CTD_human
374955  |  SPATA21  |  CTD_human
7328  |  UBE2H  |  CTD_human
388552  |  BLOC1S3  |  CTD_human
8817  |  FGF18  |  CTD_human
441151  |  TMEM151B  |  CTD_human
256472  |  TMEM151A  |  CTD_human
113251  |  LARP4  |  CTD_human
5120  |  PCOS1  |  CTD_human;OMIM
2529  |  FUT7  |  CTD_human
3976  |  LIF  |  CTD_human
9200  |  HACD1  |  CTD_human
5140  |  PDE3B  |  CTD_human
378938  |  MALAT1  |  CTD_human
114822  |  RHPN1  |  CTD_human
57731  |  SPTBN4  |  CTD_human
170394  |  PWWP2B  |  CTD_human
5862  |  RAB2A  |  CTD_human
2549  |  GAB1  |  CTD_human
91608  |  RASL10B  |  CTD_human
6939  |  TCF15  |  CTD_human
126306  |  JSRP1  |  CTD_human
7272  |  TTK  |  CTD_human
349565  |  NMNAT3  |  CTD_human
147906  |  DACT3  |  CTD_human
4544  |  MTNR1B  |  CTD_human
10454  |  TAB1  |  CTD_human
84376  |  HOOK3  |  CTD_human
7755  |  ZNF205  |  CTD_human
79906  |  MORN1  |  CTD_human
3283  |  HSD3B1  |  CTD_human
563  |  AZGP1  |  CTD_human
104  |  ADARB1  |  CTD_human
23112  |  TNRC6B  |  CTD_human
22924  |  MAPRE3  |  CTD_human
9134  |  CCNE2  |  CTD_human
151354  |  FAM84A  |  CTD_human
1995  |  ELAVL3  |  CTD_human
11173  |  ADAMTS7  |  CTD_human
4603  |  MYBL1  |  CTD_human
84909  |  C9orf3  |  GWASCAT
466  |  ATF1  |  CTD_human
57455  |  REXO1  |  CTD_human
54947  |  LPCAT2  |  CTD_human
54443  |  ANLN  |  CTD_human
57636  |  ARHGAP23  |  CTD_human
4796  |  TONSL  |  CTD_human
158314  |  LINC00475  |  CTD_human
256933  |  NPB  |  CTD_human
6343  |  SCT  |  CTD_human
1645  |  AKR1C1  |  CTD_human
1646  |  AKR1C2  |  CTD_human
7110  |  TMF1  |  CTD_human
30000  |  TNPO2  |  CTD_human
374920  |  C19orf68  |  CTD_human
146433  |  IL34  |  CTD_human
1364  |  CLDN4  |  CTD_human
23162  |  MAPK8IP3  |  CTD_human
55503  |  TRPV6  |  CTD_human
93659  |  CGB5  |  CTD_human
57706  |  DENND1A  |  GWASCAT
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:211)
3643  |  INSR  |  CIPHER
1636  |  ACE  |  CIPHER
9370  |  ADIPOQ  |  CIPHER
11132  |  CAPN10  |  CIPHER
1586  |  CYP17A1  |  CIPHER
1588  |  CYP19A1  |  CIPHER;CTD_human
55527  |  FEM1A  |  CIPHER
2488  |  FSHB  |  CIPHER
2492  |  FSHR  |  CIPHER;CTD_human
10468  |  FST  |  CIPHER;CTD_human
3667  |  IRS1  |  CIPHER
8660  |  IRS2  |  CIPHER
2908  |  NR3C1  |  CIPHER
5054  |  SERPINE1  |  CIPHER
7124  |  TNF  |  CIPHER
90  |  ACVR1  |  CIPHER
208  |  AKT2  |  CIPHER
268  |  AMH  |  CIPHER
269  |  AMHR2  |  CIPHER
367  |  AR  |  CIPHER
1020  |  CDK5  |  CIPHER
54901  |  CDKAL1  |  CIPHER
1583  |  CYP11A1  |  CIPHER
1585  |  CYP11B2  |  CIPHER
1543  |  CYP1A1  |  CIPHER
1559  |  CYP2C9  |  CIPHER
1565  |  CYP2D6  |  CIPHER
1551  |  CYP3A7  |  CIPHER
57706  |  DENND1A  |  CIPHER
1814  |  DRD3  |  CIPHER
5167  |  ENPP1  |  CIPHER
2052  |  EPHX1  |  CIPHER
2099  |  ESR1  |  CIPHER
2100  |  ESR2  |  CIPHER
84467  |  FBN3  |  CIPHER
79068  |  FTO  |  CIPHER
51738  |  GHRL  |  CIPHER
2932  |  GSK3B  |  CIPHER
9563  |  H6PD  |  CIPHER
3087  |  HHEX  |  CIPHER
3290  |  HSD11B1  |  CIPHER
8630  |  HSD17B6  |  CIPHER
3283  |  HSD3B1  |  CIPHER;CTD_human
3416  |  IDE  |  CIPHER
3557  |  IL1RN  |  CIPHER
3569  |  IL6  |  CIPHER
3630  |  INS  |  CIPHER;CTD_human
3973  |  LHCGR  |  CIPHER
4000  |  LMNA  |  CIPHER;CTD_human
4041  |  LRP5  |  CIPHER
23101  |  MCF2L2  |  CIPHER
4312  |  MMP1  |  CIPHER
4524  |  MTHFR  |  CIPHER
4548  |  MTR  |  CIPHER
4846  |  NOS3  |  CIPHER
5151  |  PDE8A  |  CIPHER
5295  |  PIK3R1  |  CIPHER
5465  |  PPARA  |  CIPHER
5467  |  PPARD  |  CIPHER
5468  |  PPARG  |  CIPHER
10891  |  PPARGC1A  |  CIPHER
6462  |  SHBG  |  CIPHER
169026  |  SLC30A8  |  CIPHER
6794  |  STK11  |  CIPHER
286749  |  STON1-GTF2A1L  |  CIPHER
412  |  STS  |  CIPHER
6822  |  SULT2A1  |  CIPHER
6934  |  TCF7L2  |  CIPHER
63892  |  THADA  |  CIPHER
7422  |  VEGFA  |  CIPHER
3953  |  LEPR  |  CIPHER
3972  |  LHB  |  CTD_human
79039  |  DDX54  |  CTD_human
80127  |  CCDC176  |  CTD_human
54206  |  ERRFI1  |  CTD_human
57104  |  PNPLA2  |  CTD_human
55783  |  CMTR2  |  CTD_human
116840  |  CNTROB  |  CTD_human
2661  |  GDF9  |  CTD_human
6168  |  RPL37A  |  CTD_human
5724  |  PTAFR  |  CTD_human
10058  |  ABCB6  |  CTD_human
6899  |  TBX1  |  CTD_human
1164  |  CKS2  |  CTD_human
596  |  BCL2  |  CTD_human
2778  |  GNAS  |  CTD_human
6241  |  RRM2  |  CTD_human
164395  |  TTLL9  |  CTD_human
891  |  CCNB1  |  CTD_human
6102  |  RP2  |  CTD_human
3070  |  HELLS  |  CTD_human
144577  |  C12orf66  |  CTD_human
23658  |  LSM5  |  CTD_human
9210  |  BMP15  |  CTD_human
817  |  CAMK2D  |  CTD_human
3977  |  LIFR  |  CTD_human
9205  |  ZMYM5  |  CTD_human
6286  |  S100P  |  CTD_human
1756  |  DMD  |  CTD_human
653545  |  DUX4L5  |  CTD_human
338324  |  S100A7A  |  CTD_human
864  |  RUNX3  |  CTD_human
4058  |  LTK  |  CTD_human
440836  |  ODF3B  |  CTD_human
8644  |  AKR1C3  |  CTD_human
55721  |  IQCC  |  CTD_human
257106  |  ARHGAP30  |  CTD_human
171558  |  PTCRA  |  CTD_human
93611  |  FBXO44  |  CTD_human
90326  |  THAP3  |  CTD_human
79685  |  SAP30L  |  CTD_human
57449  |  PLEKHG5  |  CTD_human
131566  |  DCBLD2  |  CTD_human
29127  |  RACGAP1  |  CTD_human
6770  |  STAR  |  CTD_human
10772  |  SRSF10  |  CTD_human
79694  |  MANEA  |  CTD_human
4085  |  MAD2L1  |  CTD_human
80264  |  ZNF430  |  CTD_human
3500  |  IGHG1  |  CTD_human
1742  |  DLG4  |  CTD_human
3850  |  KRT3  |  CTD_human
8463  |  TEAD2  |  CTD_human
7037  |  TFRC  |  CTD_human
29997  |  GLTSCR2  |  CTD_human
6440  |  SFTPC  |  CTD_human
23671  |  TMEFF2  |  CTD_human
347088  |  GPR144  |  CTD_human
146664  |  MGAT5B  |  CTD_human
51477  |  ISYNA1  |  CTD_human
8572  |  PDLIM4  |  CTD_human
3952  |  LEP  |  CTD_human
374955  |  SPATA21  |  CTD_human
7328  |  UBE2H  |  CTD_human
388552  |  BLOC1S3  |  CTD_human
50943  |  FOXP3  |  CTD_human
8817  |  FGF18  |  CTD_human
441151  |  TMEM151B  |  CTD_human
256472  |  TMEM151A  |  CTD_human
5950  |  RBP4  |  CTD_human
113251  |  LARP4  |  CTD_human
5120  |  PCOS1  |  CTD_human
2529  |  FUT7  |  CTD_human
3976  |  LIF  |  CTD_human
3084  |  NRG1  |  CTD_human
90668  |  LRRC16B  |  CTD_human
5140  |  PDE3B  |  CTD_human
378938  |  MALAT1  |  CTD_human
56946  |  C11orf30  |  CTD_human
114822  |  RHPN1  |  CTD_human
57731  |  SPTBN4  |  CTD_human
170394  |  PWWP2B  |  CTD_human
5862  |  RAB2A  |  CTD_human
2549  |  GAB1  |  CTD_human
91608  |  RASL10B  |  CTD_human
6939  |  TCF15  |  CTD_human
126306  |  JSRP1  |  CTD_human
55872  |  PBK  |  CTD_human
3161  |  HMMR  |  CTD_human
349565  |  NMNAT3  |  CTD_human
147906  |  DACT3  |  CTD_human
2812  |  GP1BB  |  CTD_human
5733  |  PTGER3  |  CTD_human
10454  |  TAB1  |  CTD_human
84376  |  HOOK3  |  CTD_human
7755  |  ZNF205  |  CTD_human
79906  |  MORN1  |  CTD_human
6715  |  SRD5A1  |  CTD_human
53335  |  BCL11A  |  CTD_human
6665  |  SOX15  |  CTD_human
7272  |  TTK  |  CTD_human
563  |  AZGP1  |  CTD_human
104  |  ADARB1  |  CTD_human
23112  |  TNRC6B  |  CTD_human
22924  |  MAPRE3  |  CTD_human
9134  |  CCNE2  |  CTD_human
151354  |  FAM84A  |  CTD_human
259266  |  ASPM  |  CTD_human
1995  |  ELAVL3  |  CTD_human
11173  |  ADAMTS7  |  CTD_human
4603  |  MYBL1  |  CTD_human
3284  |  HSD3B2  |  CTD_human
466  |  ATF1  |  CTD_human
57455  |  REXO1  |  CTD_human
25865  |  PRKD2  |  CTD_human
54947  |  LPCAT2  |  CTD_human
57636  |  ARHGAP23  |  CTD_human
2324  |  FLT4  |  CTD_human
4796  |  TONSL  |  CTD_human
581  |  BAX  |  CTD_human
158314  |  LINC00475  |  CTD_human
256933  |  NPB  |  CTD_human
6343  |  SCT  |  CTD_human
1645  |  AKR1C1  |  CTD_human
1646  |  AKR1C2  |  CTD_human
7110  |  TMF1  |  CTD_human
990  |  CDC6  |  CTD_human
30000  |  TNPO2  |  CTD_human
374920  |  C19orf68  |  CTD_human
55165  |  CEP55  |  CTD_human
9200  |  HACD1  |  CTD_human
146433  |  IL34  |  CTD_human
54443  |  ANLN  |  CTD_human
1364  |  CLDN4  |  CTD_human
23162  |  MAPK8IP3  |  CTD_human
55503  |  TRPV6  |  CTD_human
6337  |  SCNN1A  |  CTD_human
4544  |  MTNR1B  |  CTD_human
7153  |  TOP2A  |  CTD_human
1013  |  CDH15  |  CTD_human
93659  |  CGB5  |  CTD_human
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:130)
60  |  ACTB  |  1.032  |  DISEASES
81569  |  ACTL8  |  2.348  |  DISEASES
56999  |  ADAMTS9  |  1.181  |  DISEASES
9370  |  ADIPOQ  |  5.028  |  DISEASES
51094  |  ADIPOR1  |  2.981  |  DISEASES
79602  |  ADIPOR2  |  2.912  |  DISEASES
155  |  ADRB3  |  1.311  |  DISEASES
1645  |  AKR1C1  |  1.15  |  DISEASES
8644  |  AKR1C3  |  2.826  |  DISEASES
208  |  AKT2  |  1.791  |  DISEASES
223  |  ALDH9A1  |  1.056  |  DISEASES
164  |  AP1G1  |  1.732  |  DISEASES
375318  |  AQP12A  |  1.269  |  DISEASES
367  |  AR  |  3.876  |  DISEASES
10139  |  ARFRP1  |  1.503  |  DISEASES
632  |  BGLAP  |  1.107  |  DISEASES
353500  |  BMP8A  |  1.437  |  DISEASES
84909  |  C9orf3  |  3.329  |  DISEASES
11132  |  CAPN10  |  3.98  |  DISEASES
885  |  CCK  |  1.156  |  DISEASES
2826  |  CCR10  |  1.735  |  DISEASES
1675  |  CFD  |  1.443  |  DISEASES
7555  |  CNBP  |  1.431  |  DISEASES
22796  |  COG2  |  3.16  |  DISEASES
1312  |  COMT  |  1.328  |  DISEASES
1528  |  CYB5A  |  1.854  |  DISEASES
1586  |  CYP17A1  |  5.594  |  DISEASES
1543  |  CYP1A1  |  1.783  |  DISEASES
1589  |  CYP21A2  |  3.772  |  DISEASES
57706  |  DENND1A  |  5.602  |  DISEASES
1906  |  EDN1  |  2.413  |  DISEASES
375704  |  ENHO  |  1.875  |  DISEASES
2100  |  ESR2  |  2.466  |  DISEASES
2159  |  F10  |  2.238  |  DISEASES
2152  |  F3  |  1.418  |  DISEASES
388581  |  FAM132A  |  1.909  |  DISEASES
26232  |  FBXO2  |  1.132  |  DISEASES
2274  |  FHL2  |  2.639  |  DISEASES
252995  |  FNDC5  |  2.676  |  DISEASES
2308  |  FOXO1  |  1.432  |  DISEASES
2492  |  FSHR  |  4.943  |  DISEASES
79068  |  FTO  |  3.117  |  DISEASES
85569  |  GALP  |  1.222  |  DISEASES
2626  |  GATA4  |  1.182  |  DISEASES
2641  |  GCG  |  2.221  |  DISEASES
51738  |  GHRL  |  3.978  |  DISEASES
2879  |  GPX4  |  1.38  |  DISEASES
2932  |  GSK3B  |  1.184  |  DISEASES
51527  |  GSKIP  |  1.423  |  DISEASES
9563  |  H6PD  |  3.262  |  DISEASES
9464  |  HAND2  |  1.183  |  DISEASES
3055  |  HCK  |  1.196  |  DISEASES
85441  |  HELZ2  |  1.617  |  DISEASES
57801  |  HES4  |  1.076  |  DISEASES
64344  |  HIF3A  |  1.055  |  DISEASES
3198  |  HOXA1  |  1.901  |  DISEASES
3240  |  HP  |  1.222  |  DISEASES
3292  |  HSD17B1  |  1.171  |  DISEASES
345275  |  HSD17B13  |  1.262  |  DISEASES
3293  |  HSD17B3  |  1.178  |  DISEASES
3283  |  HSD3B1  |  3.964  |  DISEASES
3284  |  HSD3B2  |  3.856  |  DISEASES
3481  |  IGF2  |  3.085  |  DISEASES
3486  |  IGFBP3  |  3.374  |  DISEASES
3547  |  IGSF1  |  1.513  |  DISEASES
3640  |  INSL3  |  2.939  |  DISEASES
8660  |  IRS2  |  3.604  |  DISEASES
55600  |  ITLN1  |  3.72  |  DISEASES
3767  |  KCNJ11  |  1.93  |  DISEASES
3814  |  KISS1  |  3.753  |  DISEASES
7044  |  LEFTY2  |  1.772  |  DISEASES
3953  |  LEPR  |  2.424  |  DISEASES
4000  |  LMNA  |  2.611  |  DISEASES
4018  |  LPA  |  2.176  |  DISEASES
4052  |  LTBP1  |  1.17  |  DISEASES
23101  |  MCF2L2  |  1.394  |  DISEASES
4318  |  MMP9  |  1.767  |  DISEASES
4524  |  MTHFR  |  2.4  |  DISEASES
2475  |  MTOR  |  1.226  |  DISEASES
8202  |  NCOA3  |  1.204  |  DISEASES
4700  |  NDUFA6  |  1.329  |  DISEASES
257194  |  NEGR1  |  1.76  |  DISEASES
4803  |  NGF  |  2.691  |  DISEASES
594857  |  NPS  |  1.204  |  DISEASES
2516  |  NR5A1  |  2.223  |  DISEASES
2494  |  NR5A2  |  1.254  |  DISEASES
25936  |  NSL1  |  1.923  |  DISEASES
4925  |  NUCB2  |  1.743  |  DISEASES
9060  |  PAPSS2  |  1.737  |  DISEASES
8682  |  PEA15  |  1.993  |  DISEASES
5241  |  PGR  |  1.803  |  DISEASES
80012  |  PHC3  |  1.182  |  DISEASES
100996331  |  POTEB  |  2.175  |  DISEASES
10549  |  PRDX4  |  1.008  |  DISEASES
5562  |  PRKAA1  |  1.088  |  DISEASES
5563  |  PRKAA2  |  1.425  |  DISEASES
5618  |  PRLR  |  1.707  |  DISEASES
5697  |  PYY  |  1.84  |  DISEASES
5869  |  RAB5B  |  3.588  |  DISEASES
5950  |  RBP4  |  3.317  |  DISEASES
374897  |  SBSN  |  1.289  |  DISEASES
6401  |  SELE  |  1.321  |  DISEASES
145264  |  SERPINA12  |  3.019  |  DISEASES
866  |  SERPINA6  |  1.713  |  DISEASES
6424  |  SFRP4  |  1.876  |  DISEASES
9467  |  SH3BP5  |  2.137  |  DISEASES
51100  |  SH3GLB1  |  1.193  |  DISEASES
6462  |  SHBG  |  7.428  |  DISEASES
114132  |  SIGLEC11  |  1.439  |  DISEASES
6513  |  SLC2A1  |  1.093  |  DISEASES
6517  |  SLC2A4  |  3.383  |  DISEASES
11182  |  SLC2A6  |  1.34  |  DISEASES
29988  |  SLC2A8  |  1.519  |  DISEASES
146802  |  SLC47A2  |  1.169  |  DISEASES
28232  |  SLCO3A1  |  1.906  |  DISEASES
9021  |  SOCS3  |  1.088  |  DISEASES
10580  |  SORBS1  |  1.918  |  DISEASES
80320  |  SP6  |  2.512  |  DISEASES
6710  |  SPTB  |  1.797  |  DISEASES
79987  |  SVEP1  |  1.256  |  DISEASES
9882  |  TBC1D4  |  2.774  |  DISEASES
6934  |  TCF7L2  |  2.904  |  DISEASES
7062  |  TCHH  |  2.587  |  DISEASES
63892  |  THADA  |  4.177  |  DISEASES
7124  |  TNF  |  3.095  |  DISEASES
23043  |  TNIK  |  1.599  |  DISEASES
9736  |  USP34  |  3.569  |  DISEASES
7421  |  VDR  |  2.041  |  DISEASES
7422  |  VEGFA  |  2.27  |  DISEASES
168374  |  ZNF92  |  1.617  |  DISEASES
Locus(Waiting for update.)
Disease ID 41
Disease polycystic ovary syndrome
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:6)
HP:0008675  |  Enlarged polycystic ovaries
HP:0000141  |  Abnormal absence of menstruation
HP:0001513  |  Obesity
HP:0001939  |  Laboratory abnormality
HP:0001007  |  Hirsutism
HP:0000876  |  Oligomenorrhea
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:86)
HP:0000855  |  Insulin resistance  |  148
HP:0001513  |  Obesity  |  70
HP:0000789  |  Infertility  |  65
HP:0001007  |  Hirsutism  |  26
HP:0000842  |  Elevated insulin level  |  17
HP:0000716  |  Depression  |  16
HP:0000819  |  Diabetes mellitus  |  16
HP:0000822  |  Hypertension  |  15
HP:0001061  |  Acne  |  13
HP:0000833  |  Glucose intolerance  |  10
HP:0000141  |  Abnormal absence of menstruation  |  9
HP:0012743  |  Central obesity  |  8
HP:0001397  |  Hepatic steatosis  |  8
HP:0009800  |  gestational diabetes  |  8
HP:0000876  |  Oligomenorrhea  |  7
HP:0001824  |  Weight loss  |  7
HP:0000138  |  Ovarian cyst  |  7
HP:0000147  |  Sclerocystic ovaries  |  7
HP:0003251  |  Male infertility  |  6
HP:0002960  |  Autoimmune condition  |  6
HP:0000821  |  Underactive thyroid  |  6
HP:0008222  |  Female infertility  |  6
HP:0100646  |  Thyroiditis  |  5
HP:0000739  |  Anxiety  |  5
HP:0000858  |  Menstrual irregularity  |  4
HP:0100512  |  Vitamin D deficiency  |  4
HP:0100602  |  Pre-eclampsia  |  4
HP:0000869  |  Secondary amenorrhea  |  3
HP:0003002  |  Breast carcinoma  |  3
HP:0000870  |  Hyperprolactinemia  |  3
HP:0002621  |  Atherosclerosis  |  3
HP:0002870  |  Obstructive sleep apnea  |  2
HP:0007302  |  Bipolar disorder  |  2
HP:0000853  |  Goitre  |  2
HP:0009125  |  Lipodystrophy  |  2
HP:0002516  |  Intracranial pressure elevation  |  2
HP:0001297  |  Cerebral vascular events  |  2
HP:0002459  |  Dysautonomia  |  2
HP:0000144  |  Decreased fertility  |  2
HP:0001622  |  Premature delivery  |  2
HP:0000832  |  Primary hypothyroidism  |  2
HP:0001596  |  Hair loss  |  2
HP:0005268  |  Spontaneous abortion  |  2
HP:0006279  |  Beta-cell dysfunction  |  2
HP:0001952  |  Abnormal glucose tolerance  |  2
HP:0100601  |  Eclampsia  |  2
HP:0012594  |  High urine albumin levels  |  1
HP:0001894  |  Thrombocytosis  |  1
HP:0003765  |  Psoriasis  |  1
HP:0000820  |  Thyroid abnormality  |  1
HP:0001712  |  Left ventricular hypertrophy  |  1
HP:0002664  |  Neoplasia  |  1
HP:0000709  |  Psychosis  |  1
HP:0000998  |  Hypertrichosis  |  1
HP:0200067  |  Recurrent spontaneous abortion  |  1
HP:0040217  |  Elevated hemoglobin A1c  |  1
HP:0005543  |  Reduced protein C activity  |  1
HP:0003077  |  Hyperlipidemia  |  1
HP:0000135  |  Hypogonadism  |  1
HP:0000752  |  Hyperactive behavior  |  1
HP:0001518  |  Small for gestational age  |  1
HP:0003281  |  Increased ferritin  |  1
HP:0001717  |  Coronary artery calcification  |  1
HP:0003005  |  Ganglioneuroma  |  1
HP:0000708  |  Behavioral problems  |  1
HP:0100739  |  Binge and purge  |  1
HP:0000020  |  Bladder incontinence  |  1
HP:0000016  |  Urinary retention  |  1
HP:0000729  |  Pervasive developmental disorder  |  1
HP:0002155  |  Increased triglycerides  |  1
HP:0000726  |  Dementia  |  1
HP:0001677  |  Coronary artery disease  |  1
HP:0000826  |  Precocious puberty  |  1
HP:0001907  |  Thromboembolic disease  |  1
HP:0001714  |  Ventricular hypertrophy  |  1
HP:0004416  |  Precocious atherosclerosis  |  1
HP:0000230  |  Inflamed gums  |  1
HP:0008221  |  Enlarged adrenal glands  |  1
HP:0012114  |  Endometrial carcinoma  |  1
HP:0002360  |  Sleep disturbance  |  1
HP:0100879  |  Enlarged ovaries  |  1
HP:0100724  |  Hypercoagulability  |  1
HP:0002104  |  Absence of spontaneous respiration  |  1
HP:0010535  |  Sleep apnea  |  1
HP:0003074  |  High blood glucose  |  1
HP:0000872  |  Hashimoto's thyroiditis  |  1
Disease ID 41
Disease polycystic ovary syndrome
Manually Symptom
UMLS  | Name(Total Manually Symptoms:45)
C2697363  |  endometrial cancer
C2364072  |  depression
C2318511  |  nonalcoholic steatohepatitis
C1963185  |  obesity
C1963138  |  hypertension
C1963064  |  anxiety
C1563743  |  adiposity
C1555754  |  cardiovascular disease
C0948265  |  metabolic syndrome
C0920350  |  autoimmune thyroiditis
C0745411  |  irregular bleeding
C0729353  |  subfertility
C0549609  |  adrenal dysfunction
C0404572  |  anovulatory infertility
C0314719  |  dry eye
C0311277  |  central obesity
C0271650  |  impaired glucose tolerance
C0271650  |  glucose intolerance
C0271602  |  hypersecretion of ovarian androgens
C0242339  |  dyslipidemia
C0235461  |  androgen excess
C0235401  |  abnormal glucose tolerance
C0232919  |  infertile
C0206081  |  hyperandrogenism
C0205875  |  papillomatosis
C0154208  |  ovarian dysfunction
C0085083  |  ovarian hyperstimulation syndrome
C0037285  |  skin manifestations
C0032991  |  ovarian pregnancy
C0032460  |  polycystic ovaries
C0025517  |  metabolic disorders
C0021361  |  female infertility
C0021359  |  infertility
C0020514  |  hyperprolactinemia
C0020514  |  hyperprolactinaemia
C0020459  |  hyperinsulinism
C0020459  |  hyperinsulinemia
C0020459  |  hyperinsulinaemia
C0014173  |  endometrial hyperplasia
C0014130  |  endocrinopathy
C0014130  |  endocrine problem
C0004153  |  atherosclerosis
C0003128  |  anovulation
C0000889  |  acanthosis nigricans
C0000786  |  miscarriage
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:33)
C0021359  |  infertile  |  35
C0021359  |  infertility  |  34
C0206081  |  hyperandrogenism  |  33
C0948265  |  metabolic syndrome  |  23
C0028754  |  obesity  |  21
C0003128  |  anovulation  |  13
C0007222  |  cardiovascular disease  |  12
C0011570  |  depression  |  8
C0242339  |  dyslipidemia  |  7
C0025517  |  metabolic disorders  |  6
C0404572  |  anovulatory infertility  |  5
C0311277  |  central obesity  |  4
C0729353  |  subfertility  |  4
C0014173  |  endometrial hyperplasia  |  3
C0085083  |  ovarian hyperstimulation syndrome  |  3
C0002453  |  amenorrhea  |  3
C0020538  |  hypertension  |  3
C0159069  |  impaired glucose tolerance  |  3
C0032460  |  polycystic ovaries  |  2
C0920350  |  autoimmune thyroiditis  |  2
C0476089  |  endometrial cancer  |  2
C0021361  |  female infertility  |  2
C0235461  |  androgen excess  |  2
C0000809  |  recurrent miscarriage  |  1
C0000786  |  miscarriage  |  1
C0700502  |  primary hypothyroidism  |  1
C0549609  |  adrenal dysfunction  |  1
C0235401  |  abnormal glucose tolerance  |  1
C0154208  |  ovarian dysfunction  |  1
C0020459  |  hyperinsulinemia  |  1
C0028754  |  adiposity  |  1
C0242339  |  dyslipidaemia  |  1
C0271650  |  glucose intolerance  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:125)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1019731207340643479IGF1umls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0113544082010IGF112102470647CA
rs1048943195070641543CYP1A1umls:C0032460BeFreeLack of an association between CYP1A1 gene Ile462Val polymorphism and polycystic ovary syndrome in Chinese.0.0114540972009CYP1A11574720644TG,C,A
rs1061622121615457133TNFRSF1Bumls:C0032460BeFreeComment: the methionine 196 arginine polymorphism in exon 6 of the TNF receptor 2 gene (TNFRSF1B) is associated with the polycystic ovary syndrome and hyperandrogenism.0.0053628242002TNFRSF1B112192898TG
rs1061622121615457124TNFumls:C0032460BeFreeComment: the methionine 196 arginine polymorphism in exon 6 of the TNF receptor 2 gene (TNFRSF1B) is associated with the polycystic ovary syndrome and hyperandrogenism.0.0126257412002TNFRSF1B112192898TG
rs1073768207340642691GHRHumls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0023670322010NA2037248607TC
rs108188542115112857706DENND1Aumls:C0032460GWASCATGenome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.0.1245385672011DENND1A9123684499GA
rs108188542115112857706DENND1Aumls:C0032460GAD[Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.]0.1245385672011DENND1A9123684499GA
rs10830962209593874544MTNR1Bumls:C0032460BeFreeAssociation of rs10830963 and rs10830962 SNPs in the melatonin receptor (MTNR1B) gene among Han Chinese women with polycystic ovary syndrome.0.1229099162011NA1192965261CG
rs10830963209593874544MTNR1Bumls:C0032460BeFreeAssociation of rs10830963 and rs10830962 SNPs in the melatonin receptor (MTNR1B) gene among Han Chinese women with polycystic ovary syndrome.0.1229099162011MTNR1B1192975544CG
rs1111875200412873630INSumls:C0032460BeFreeThis study was to evaluate whether polymorphisms of TCF7L2 (rs7903146) and HHEX (rs1111875) genes responsible for insulin secretion are associated with the polycystic ovary syndrome (PCOS) in Chinese people.0.1616277522010NA1092703125CT
rs124786012115112863892THADAumls:C0032460GWASCATGenome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.0.1234527992011THADA243494369CT
rs124786012115112863892THADAumls:C0032460GAD[Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.]0.1234527992011THADA243494369CT
rs13405728229029183973LHCGRumls:C0032460BeFreeThe aim of this study was to explore the polycystic ovary syndrome (PCOS) related single nucleotide polymorphisms (SNPs) rs13405728 (in gene LHCGR), rs13429458 (in gene THADA) and rs2479106 (in gene DENND1A) in women with endometrial carcinoma.0.1295440732012LHCGR;STON1-GTF2A1L248751020AG
rs134057282290291857706DENND1Aumls:C0032460BeFreeThe aim of this study was to explore the polycystic ovary syndrome (PCOS) related single nucleotide polymorphisms (SNPs) rs13405728 (in gene LHCGR), rs13429458 (in gene THADA) and rs2479106 (in gene DENND1A) in women with endometrial carcinoma.0.1245385672012LHCGR;STON1-GTF2A1L248751020AG
rs13405728211511283973LHCGRumls:C0032460GWASCATGenome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.0.1295440732011LHCGR;STON1-GTF2A1L248751020AG
rs1340572821151128286749STON1-GTF2A1Lumls:C0032460GWASCATGenome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.0.122011LHCGR;STON1-GTF2A1L248751020AG
rs13405728228859253973LHCGRumls:C0032460GWASCATGenome-wide association study identifies eight new risk loci for polycystic ovary syndrome.0.1295440732012LHCGR;STON1-GTF2A1L248751020AG
rs1340572822885925286749STON1-GTF2A1Lumls:C0032460GWASCATGenome-wide association study identifies eight new risk loci for polycystic ovary syndrome.0.122012LHCGR;STON1-GTF2A1L248751020AG
rs134057282290291863892THADAumls:C0032460BeFreeThe aim of this study was to explore the polycystic ovary syndrome (PCOS) related single nucleotide polymorphisms (SNPs) rs13405728 (in gene LHCGR), rs13429458 (in gene THADA) and rs2479106 (in gene DENND1A) in women with endometrial carcinoma.0.1234527992012LHCGR;STON1-GTF2A1L248751020AG
rs13405728211511283973LHCGRumls:C0032460GAD[Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.]0.1295440732011LHCGR;STON1-GTF2A1L248751020AG
rs134294582115112863892THADAumls:C0032460GWASCATGenome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.0.1234527992011THADA243411699AC
rs134294582290291857706DENND1Aumls:C0032460BeFreeThe aim of this study was to explore the polycystic ovary syndrome (PCOS) related single nucleotide polymorphisms (SNPs) rs13405728 (in gene LHCGR), rs13429458 (in gene THADA) and rs2479106 (in gene DENND1A) in women with endometrial carcinoma.0.1245385672012THADA243411699AC
rs134294582290291863892THADAumls:C0032460BeFreeThe aim of this study was to explore the polycystic ovary syndrome (PCOS) related single nucleotide polymorphisms (SNPs) rs13405728 (in gene LHCGR), rs13429458 (in gene THADA) and rs2479106 (in gene DENND1A) in women with endometrial carcinoma.0.1234527992012THADA243411699AC
rs134294582115112863892THADAumls:C0032460GAD[Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.]0.1234527992011THADA243411699AC
rs13429458229029183973LHCGRumls:C0032460BeFreeThe aim of this study was to explore the polycystic ovary syndrome (PCOS) related single nucleotide polymorphisms (SNPs) rs13405728 (in gene LHCGR), rs13429458 (in gene THADA) and rs2479106 (in gene DENND1A) in women with endometrial carcinoma.0.1295440732012THADA243411699AC
rs134294582288592563892THADAumls:C0032460GWASCATGenome-wide association study identifies eight new risk loci for polycystic ovary syndrome.0.1234527992012THADA243411699AC
rs1590207340647040TGFB1umls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0029099162010TGFBR1999153883TG
rs1799817192117083643INSRumls:C0032460GAD[Genetic variation in exon 17 of INSR is associated with insulin resistance and hyperandrogenemia among lean Indian women with polycystic ovary syndrome.]0.1598010612009INSR197125286GA
rs1800447251111163972LHBumls:C0032460BeFreeTrp28Arg/Ile35Thr LHB gene variants are associated with elevated testosterone levels in women with polycystic ovary syndrome.0.1208143262014LHB1949016648AG
rs1801276166030553667IRS1umls:C0032460BeFreeAbnormal glucose tolerance and insulin resistance in polycystic ovary syndrome amongst the Taiwanese population- not correlated with insulin receptor substrate-1 Gly972Arg/Ala513Pro polymorphism.0.0441877382006IRS12226797205CG
rs1801278154748803630INSumls:C0032460BeFreeInsulin secretion in women who have polycystic ovary syndrome and carry the Gly972Arg variant of insulin receptor substrate-1 in response to a high-glycemic or low-glycemic carbohydrate load.0.1616277522004IRS12226795828CT,G,A
rs1801278115226863667IRS1umls:C0032460BeFreeRole of allelic variants Gly972Arg of IRS-1 and Gly1057Asp of IRS-2 in moderate-to-severe insulin resistance of women with polycystic ovary syndrome.0.0441877382001IRS12226795828CT,G,A
rs1801278115226868660IRS2umls:C0032460BeFreeRole of allelic variants Gly972Arg of IRS-1 and Gly1057Asp of IRS-2 in moderate-to-severe insulin resistance of women with polycystic ovary syndrome.0.0114540972001IRS12226795828CT,G,A
rs1801278166030553667IRS1umls:C0032460BeFreeAbnormal glucose tolerance and insulin resistance in polycystic ovary syndrome amongst the Taiwanese population- not correlated with insulin receptor substrate-1 Gly972Arg/Ala513Pro polymorphism.0.0441877382006IRS12226795828CT,G,A
rs1801278160848823667IRS1umls:C0032460BeFreeAssociation of Gly972Arg variant of insulin receptor substrate-1 with metabolic features in women with polycystic ovary syndrome.0.0441877382005IRS12226795828CT,G,A
rs1801278201703523667IRS1umls:C0032460BeFreeTo assess the prevalence of IRS-1 Gly972Arg and GNB3 C825T polymorphisms in women with polycystic ovary syndrome (PCOS) and their relation to the metabolic syndrome and hyperandrogenaemia.0.0441877382010IRS12226795828CT,G,A
rs1801278201703522784GNB3umls:C0032460BeFreeTo assess the prevalence of IRS-1 Gly972Arg and GNB3 C825T polymorphisms in women with polycystic ovary syndrome (PCOS) and their relation to the metabolic syndrome and hyperandrogenaemia.0.0026384742010IRS12226795828CT,G,A
rs1801278182221203667IRS1umls:C0032460BeFreeNo association between common Gly972Arg variant of the insulin receptor substrate-1 and polycystic ovary syndrome in Southern Chilean women.0.0441877382008IRS12226795828CT,G,A
rs1801278202294503667IRS1umls:C0032460BeFreeVery high frequency of the polymorphism for the insulin receptor substrate 1 (IRS-1) at codon 972 (glycine972arginine) in Southern Italian women with polycystic ovary syndrome.0.0441877382010IRS12226795828CT,G,A
rs1801278154748803667IRS1umls:C0032460BeFreeInsulin secretion in women who have polycystic ovary syndrome and carry the Gly972Arg variant of insulin receptor substrate-1 in response to a high-glycemic or low-glycemic carbohydrate load.0.0441877382004IRS12226795828CT,G,A
rs1801278156650223667IRS1umls:C0032460BeFreeThe importance of IRS-1 Gly972Arg polymorphism in evaluating the response to metformin treatment in polycystic ovary syndrome.0.0441877382005IRS12226795828CT,G,A
rs1801282118363195468PPARGumls:C0032460BeFreeInsulin resistance is attenuated in women with polycystic ovary syndrome with the Pro(12)Ala polymorphism in the PPARgamma gene.0.0617430412002PPARG312351626CG
rs1801282118363193630INSumls:C0032460BeFreeInsulin resistance is attenuated in women with polycystic ovary syndrome with the Pro(12)Ala polymorphism in the PPARgamma gene.0.1616277522002PPARG312351626CG
rs1801282227299155468PPARGumls:C0032460BeFreeAssociation of Pro12Ala polymorphism in peroxisome proliferator-activated receptor gamma with polycystic ovary syndrome: a meta-analysis.0.0617430412012PPARG312351626CG
rs1801282167851595468PPARGumls:C0032460BeFreePro12Ala polymorphism of the peroxisome proliferator-activated receptor-gamma gene in women with polycystic ovary syndrome.0.0617430412006PPARG312351626CG
rs1801282163168415468PPARGumls:C0032460BeFreePro12Ala polymorphism of the peroxisome proliferator-activated receptor-gamma gene in first-degree relatives of subjects with polycystic ovary syndrome.0.0617430412005PPARG312351626CG
rs1801282227299155465PPARAumls:C0032460BeFreeThe association between Pro12Ala polymorphism in peroxisome proliferator-activated receptor gamma (PPAR) and polycystic ovary syndrome (PCOS) has been investigated in several studies, whereas results were often incompatible.0.0031813582012PPARG312351626CG
rs1801282225279033630INSumls:C0032460BeFreeTo investigate the influence of the peroxisome proliferator activated receptor gamma (PPAR-γ) Pro12Ala polymorphism on the susceptibility of polycystic ovary syndrome (PCOS) and body mass index (BMI), fast insulin levels, homeostasis model assessment of insulin resistance (HOMA-IR) in PCOS patients.0.1616277522012PPARG312351626CG
rs1801282225279035468PPARGumls:C0032460BeFreeA meta-analysis on the association between PPAR-γ Pro12Ala polymorphism and polycystic ovary syndrome.0.0617430412012PPARG312351626CG
rs1801282158538275468PPARGumls:C0032460BeFreeThe peroxisome proliferator activated receptor gamma Pro12Ala polymorphism is associated with a lower hirsutism score and increased insulin sensitivity in women with polycystic ovary syndrome.0.0617430412005PPARG312351626CG
rs1801282154722145468PPARGumls:C0032460BeFreeLack of an association between peroxisome proliferator-activated receptor-gamma gene Pro12Ala polymorphism and adiponectin levels in the polycystic ovary syndrome.0.0617430412004PPARG312351626CG
rs1801282225647025468PPARGumls:C0032460BeFreeAssociation between the Pro12Ala polymorphism of PPAR-γ gene and the polycystic ovary syndrome: a meta-analysis of case-control studies.0.0617430412012PPARG312351626CG
rs1805097115226863667IRS1umls:C0032460BeFreeRole of allelic variants Gly972Arg of IRS-1 and Gly1057Asp of IRS-2 in moderate-to-severe insulin resistance of women with polycystic ovary syndrome.0.0441877382001IRS213109782884CT
rs1805097115226868660IRS2umls:C0032460BeFreeRole of allelic variants Gly972Arg of IRS-1 and Gly1057Asp of IRS-2 in moderate-to-severe insulin resistance of women with polycystic ovary syndrome.0.0114540972001IRS213109782884CT
rs1805192225279035468PPARGumls:C0032460BeFreeA meta-analysis on the association between PPAR-γ Pro12Ala polymorphism and polycystic ovary syndrome.0.0617430412012PPARG312379739CG
rs1805192227299155465PPARAumls:C0032460BeFreeThe association between Pro12Ala polymorphism in peroxisome proliferator-activated receptor gamma (PPAR) and polycystic ovary syndrome (PCOS) has been investigated in several studies, whereas results were often incompatible.0.0031813582012PPARG312379739CG
rs1805192225647025468PPARGumls:C0032460BeFreeAssociation between the Pro12Ala polymorphism of PPAR-γ gene and the polycystic ovary syndrome: a meta-analysis of case-control studies.0.0617430412012PPARG312379739CG
rs1805192227299155468PPARGumls:C0032460BeFreeAssociation of Pro12Ala polymorphism in peroxisome proliferator-activated receptor gamma with polycystic ovary syndrome: a meta-analysis.0.0617430412012PPARG312379739CG
rs1805192118363195468PPARGumls:C0032460BeFreeInsulin resistance is attenuated in women with polycystic ovary syndrome with the Pro(12)Ala polymorphism in the PPARgamma gene.0.0617430412002PPARG312379739CG
rs1805192225279033630INSumls:C0032460BeFreeTo investigate the influence of the peroxisome proliferator activated receptor gamma (PPAR-γ) Pro12Ala polymorphism on the susceptibility of polycystic ovary syndrome (PCOS) and body mass index (BMI), fast insulin levels, homeostasis model assessment of insulin resistance (HOMA-IR) in PCOS patients.0.1616277522012PPARG312379739CG
rs1805192158538275468PPARGumls:C0032460BeFreeThe peroxisome proliferator activated receptor gamma Pro12Ala polymorphism is associated with a lower hirsutism score and increased insulin sensitivity in women with polycystic ovary syndrome.0.0617430412005PPARG312379739CG
rs1805192167851595468PPARGumls:C0032460BeFreePro12Ala polymorphism of the peroxisome proliferator-activated receptor-gamma gene in women with polycystic ovary syndrome.0.0617430412006PPARG312379739CG
rs1805192118363193630INSumls:C0032460BeFreeInsulin resistance is attenuated in women with polycystic ovary syndrome with the Pro(12)Ala polymorphism in the PPARgamma gene.0.1616277522002PPARG312379739CG
rs1805192163168415468PPARGumls:C0032460BeFreePro12Ala polymorphism of the peroxisome proliferator-activated receptor-gamma gene in first-degree relatives of subjects with polycystic ovary syndrome.0.0617430412005PPARG312379739CG
rs1805192154722145468PPARGumls:C0032460BeFreeLack of an association between peroxisome proliferator-activated receptor-gamma gene Pro12Ala polymorphism and adiponectin levels in the polycystic ovary syndrome.0.0617430412004PPARG312379739CG
rs18941162288592510413YAP1umls:C0032460GWASCATGenome-wide association study identifies eight new risk loci for polycystic ovary syndrome.0.1202714422012YAP111102199908AG
rs2013573207340647363UGT2B4umls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0023670322010UGT2B4469488760CT
rs2059807228859253643INSRumls:C0032460GWASCATGenome-wide association study identifies eight new risk loci for polycystic ovary syndrome.0.1598010612012INSR197166098AG
rs2164808207340645443POMCumls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0063627152010EFR3B225154307TC,A
rs22417661517866154567DLL4umls:C0032460BeFreeAssociation of the T45G polymorphism in exon 2 of the adiponectin gene with polycystic ovary syndrome: role of Delta4-androstenedione.0.0002714422004ADIPOQ;ADIPOQ-AS13186853103TG
rs2241766151786619370ADIPOQumls:C0032460BeFreeAssociation of the T45G polymorphism in exon 2 of the adiponectin gene with polycystic ovary syndrome: role of Delta4-androstenedione.0.0428788492004ADIPOQ;ADIPOQ-AS13186853103TG
rs2241766236858849370ADIPOQumls:C0032460BeFreeHaplotype TGTG from SNP 45T/G and 276G/T of the adiponectin gene contributes to risk of polycystic ovary syndrome.0.0428788492014ADIPOQ;ADIPOQ-AS13186853103TG
rs2268361228859252492FSHRumls:C0032460GWASCATIn addition to confirming the three loci we previously reported, we identify eight new PCOS association signals at P < 5 × 10(-8): 9q22.32, 11q22.1, 12q13.2, 12q14.3, 16q12.1, 19p13.3, 20q13.2 and a second independent signal at 2p16.3 (the FSHR gene).0.2626268212012FSHR248974473CT
rs2272046228859258091HMGA2umls:C0032460GWASCATGenome-wide association study identifies eight new risk loci for polycystic ovary syndrome.0.122012HMGA21265830681AC
rs2288696207340642260FGFR1umls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0023670322010FGFR1838428707GA
rs2414096200154051588CYP19A1umls:C0032460BeFreeAssociation between CYP19 gene SNP rs2414096 polymorphism and polycystic ovary syndrome in Chinese women.0.2281851432009CYP19A1;PIRC661551237582GA
rs2470152219720041588CYP19A1umls:C0032460BeFreeSNP rs2470152 in CYP19 is correlated to aromatase activity in Chinese polycystic ovary syndrome patients.0.2281851432012CYP19A1;PIRC661551302775GA
rs24791062115112857706DENND1Aumls:C0032460GAD[Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.]0.1245385672011DENND1A9123762933AG
rs24791062290291857706DENND1Aumls:C0032460BeFreeThe aim of this study was to explore the polycystic ovary syndrome (PCOS) related single nucleotide polymorphisms (SNPs) rs13405728 (in gene LHCGR), rs13429458 (in gene THADA) and rs2479106 (in gene DENND1A) in women with endometrial carcinoma.0.1245385672012DENND1A9123762933AG
rs24791062290291863892THADAumls:C0032460BeFreeThe aim of this study was to explore the polycystic ovary syndrome (PCOS) related single nucleotide polymorphisms (SNPs) rs13405728 (in gene LHCGR), rs13429458 (in gene THADA) and rs2479106 (in gene DENND1A) in women with endometrial carcinoma.0.1234527992012DENND1A9123762933AG
rs24791062288592557706DENND1Aumls:C0032460GWASCATGenome-wide association study identifies eight new risk loci for polycystic ovary syndrome.0.1245385672012DENND1A9123762933AG
rs2479106229029183973LHCGRumls:C0032460BeFreeThe aim of this study was to explore the polycystic ovary syndrome (PCOS) related single nucleotide polymorphisms (SNPs) rs13405728 (in gene LHCGR), rs13429458 (in gene THADA) and rs2479106 (in gene DENND1A) in women with endometrial carcinoma.0.1295440732012DENND1A9123762933AG
rs24791062115112857706DENND1Aumls:C0032460GWASCATGenome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.0.1245385672011DENND1A9123762933AG
rs2697679207340644683NBNumls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0023670322010NBN889937652AC
rs271924207340645122PCSK1umls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0026384742010PCSK1;LOC101929710596401720AT
rs324420236161863630INSumls:C0032460BeFreeIn the control group, carriers of the polymorphism had significantly lower insulin levels.Our data indicate that the C385A polymorphism of the fatty acid amide hydrolase gene is not a genetic susceptibility factor for the development of polycystic ovary syndrome.0.1616277522014FAAH146405089CA
rs34349826251111163972LHBumls:C0032460BeFreeTrp28Arg/Ile35Thr LHB gene variants are associated with elevated testosterone levels in women with polycystic ovary syndrome.0.1208143262014LHB1949016626AG
rs34603401223063279563H6PDumls:C0032460BeFreeThe R453Q and D151A polymorphisms of hexose-6-phosphate dehydrogenase gene (H6PD) influence the polycystic ovary syndrome (PCOS) and obesity.0.0079154222012H6PD19245386AC
rs38024572288592584909C9orf3umls:C0032460GWASCATGenome-wide association study identifies eight new risk loci for polycystic ovary syndrome.0.1202714422012C9orf3994979054GA
rs4135280207340645468PPARGumls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0617430412010PPARG312407495TC
rs43855272558678484909C9orf3umls:C0032460BeFreeEach single PCOS clinical feature had a specific genetic association, and rs4385527 in the chromosome 9 open reading frame 3 (C9orf3) conferred a particular risk to the three defined PCOS clinical features in this study, which suggested its fundamental role in the etiology of PCOS.0.1202714422015C9orf3994886305GA
rs4939833207340644092SMAD7umls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0023670322010SMAD71848941590TC
rs494958207340646715SRD5A1umls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.128272742010SRD5A156639066AT
rs4953616207340643973LHCGRumls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.1295440732010LHCGR;STON1-GTF2A1L248714289CT
rs499410689004155ADRB3umls:C0032460BeFreeTo determine if the Trp(64)Arg (W64R) variant of the beta(3)-adrenergic receptor (ADRB3) could be used as a genetic marker to define risk for polycystic ovary syndrom (PCOS) and/or obesity in children and adolescents.0.0852769482000ADRB3837966280AG
rs5443201703523667IRS1umls:C0032460BeFreeTo assess the prevalence of IRS-1 Gly972Arg and GNB3 C825T polymorphisms in women with polycystic ovary syndrome (PCOS) and their relation to the metabolic syndrome and hyperandrogenaemia.0.0441877382010GNB3;CDCA3126845711CT
rs5443201703522784GNB3umls:C0032460BeFreeTo assess the prevalence of IRS-1 Gly972Arg and GNB3 C825T polymorphisms in women with polycystic ovary syndrome (PCOS) and their relation to the metabolic syndrome and hyperandrogenaemia.0.0026384742010GNB3;CDCA3126845711CT
rs593097320734064959CD40LGumls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0023670322010CD40LGX136649989GA
rs615220450840367ARumls:C0032460GAD[, the individuals carrying the rs6152A allele had significantly higher susceptibility to polycystic ovary syndrome than those that were GG homozygotes.]0.0412678912010ARX67545785GA
rs6165235361502492FSHRumls:C0032460BeFreeAssociation study between FSHR Ala307Thr and Ser680Asn variants and polycystic ovary syndrome (PCOS) in Northern Chinese Han women.0.2626268212013FSHR248963902CT,G
rs6165217926646046BRD2umls:C0032460BeFreeFSH-receptor Ala307Thr polymorphism is associated to polycystic ovary syndrome and to a higher responsiveness to exogenous FSH in Italian women.0.0021715352011FSHR248963902CT,G
rs6165217926642492FSHRumls:C0032460BeFreeFSH-receptor Ala307Thr polymorphism is associated to polycystic ovary syndrome and to a higher responsiveness to exogenous FSH in Italian women.0.2626268212011FSHR248963902CT,G
rs6166235361502492FSHRumls:C0032460BeFreeAssociation study between FSHR Ala307Thr and Ser680Asn variants and polycystic ovary syndrome (PCOS) in Northern Chinese Han women.0.2626268212013FSHR248962782CT
rs616622429116268AMHumls:C0032460BeFreeTo determine if an association exists between the follicle-stimulating hormone receptor (FSHR) gene p.Asn680Ser polymorphism and polycystic ovary syndrome (PCOS) or with high anti-mullerian hormone (AMH) levels without PCOS.0.0291574082012FSHR248962782CT
rs6166224291162492FSHRumls:C0032460BeFreeTo determine if an association exists between the follicle-stimulating hormone receptor (FSHR) gene p.Asn680Ser polymorphism and polycystic ovary syndrome (PCOS) or with high anti-mullerian hormone (AMH) levels without PCOS.0.2626268212012FSHR248962782CT
rs627920734064255239ANKK1umls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0023670322010DRD211113410351GC
rs6471202016441589CYP21A2umls:C0032460BeFreeLack of association between CYP21 V281L variant and polycystic ovary syndrome in Italian women.0.0090870652010CYP21A2632040110GA,C,T
rs6688832158271069563H6PDumls:C0032460BeFreeThe R453Q variant in the hexose-6-phosphate dehydrogenase gene (H6PD) and 83557insA mutations in 11beta-hydroxysteroid dehydrogenase (11betaHSD) type 1 gene (HSD11B1) interact, resulting in cortisone reductase deficiency (CRD), a rare disorder characterized by a polycystic ovary syndrome (PCOS)-like phenotype.0.0079154222005H6PD19263851GA,C
rs6688832158271063290HSD11B1umls:C0032460BeFreeThe R453Q variant in the hexose-6-phosphate dehydrogenase gene (H6PD) and 83557insA mutations in 11beta-hydroxysteroid dehydrogenase (11betaHSD) type 1 gene (HSD11B1) interact, resulting in cortisone reductase deficiency (CRD), a rare disorder characterized by a polycystic ovary syndrome (PCOS)-like phenotype.0.0081868632005H6PD19263851GA,C
rs6688832223063279563H6PDumls:C0032460BeFreeThe R453Q and D151A polymorphisms of hexose-6-phosphate dehydrogenase gene (H6PD) influence the polycystic ovary syndrome (PCOS) and obesity.0.0079154222012H6PD19263851GA,C
rs6962171904999251738GHRLumls:C0032460BeFreeNo association of the Arg51Gln and Leu72Met polymorphisms of the ghrelin gene and polycystic ovary syndrome.0.0168889852009GHRL;GHRLOS310289773GT
rs705379168802295444PON1umls:C0032460BeFreeBecause serum paraoxonase activity is influenced by the -108C/T polymorphism in the PON1 gene, we studied its involvement in the decreased paraoxonase activity recently described in the polycystic ovary syndrome (PCOS).0.0090870652006PON1795324583GA
rs705702228859255869RAB5Bumls:C0032460GWASCATGenome-wide association study identifies eight new risk loci for polycystic ovary syndrome.0.122012RAB5B;SUOX1255996852AG
rs705702228859256821SUOXumls:C0032460GWASCATGenome-wide association study identifies eight new risk loci for polycystic ovary syndrome.0.122012RAB5B;SUOX1255996852AG
rs7121170628942778GNASumls:C0032460BeFreeThe CC genotype of the GNAS T393C polymorphism is associated with obesity and insulin resistance in women with polycystic ovary syndrome.0.1202714422006GNAS2058903752CT
rs743572252083011586CYP17A1umls:C0032460BeFreeAssociation of CYP17A1 gene -34T/C polymorphism with polycystic ovary syndrome in Han Chinese population.0.0307139962015CYP17A110102837395AG,T
rs743572252083011555CYP2B6umls:C0032460BeFreeTo investigate the influence of the cytochrome P450 17α (CYP17A1) gene -34T/C polymorphism in the pathogenesis of polycystic ovary syndrome (PCOS) in Han Chinese population.0.0027144192015CYP17A110102837395AG,T
rs7538038207340643814KISS1umls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0023670322010KISS11204191898AG
rs7586601207340648890EIF2B4umls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0023670322010LOC105374363227361799AG
rs7903146200412873630INSumls:C0032460BeFreeThis study was to evaluate whether polymorphisms of TCF7L2 (rs7903146) and HHEX (rs1111875) genes responsible for insulin secretion are associated with the polycystic ovary syndrome (PCOS) in Chinese people.0.1616277522010TCF7L210112998590CT
rs854560203345845444PON1umls:C0032460BeFreeThe role of chronic inflammation and Leu55Met PON1 polymorphism in the pathogenesis of polycystic ovary syndrome.0.0090870652010PON1795316772AC,G,N,T
rs909253207340647124TNFumls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0126257412010LTA;LOC100287329631572536AG
rs9457827207340643482IGF2Rumls:C0032460GAD[A large-scale candidate gene association study of age at menarche and age at natural menopause.]0.0023670322010IGF2R6160082624CT
rs99396091985984079068FTOumls:C0032460BeFreeAssociation of the common rs9939609 variant of FTO gene with polycystic ovary syndrome in Chinese women.0.0160785412009FTO1653786615TA
rs99396091985984079068FTOumls:C0032460GAD[Association of the common rs9939609 variant of FTO gene with polycystic ovary syndrome in Chinese women.]0.0160785412009FTO1653786615TA
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:139)
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
111925732rs116228357CTrs116228357221787856.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
159616910rs17118876CGrs17118876229515950.0000149NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCNA
1102184478rs11164278TCrs11164278229515950.0000468NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTNA
1156352396rs872120CTrs872120229515950.00000998NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGRHBG
1181768985rs638132GArs638132229515950.0000492NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGCACNA1E
1245246340rs6429521GArs6429521229515950.0000221NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tAEFCAB2
219629832rs17495469AGrs17495469221787852.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
231344193rs10165977AGrs10165977229515950.0000192NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tAGALNT14
243532302rs11891936CTrs11891936211511282.93E-09NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tATHADA
243548128rs17030684GArs17030684211511283.46E-07NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGTHADA
243555506rs4340576TCrs4340576211511282.71E-07NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCTHADA
243561161rs12468394CArs12468394211511281.20E-09NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tATHADA
243561161rs12468394CArs12468394228859252.45E-12NANANA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tATHADA
243638185rs7567607CTrs7567607211511281.06E-08NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTTHADA
243638838rs13429458ACrs13429458211511282.00E-23NA1.49[1.39-1.61]744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers13429458-AResearch Support, Non-U.S. Gov'tATHADA
243638838rs13429458ACrs13429458228859254.00E-13NA1.49NA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers13429458-AResearch Support, Non-U.S. Gov'tATHADA
243638855rs7568365CTrs7568365211511283.02E-08NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tT,CTHADA
243638947rs7582497TCrs7582497211511286.07E-08NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCTHADA
243648176rs10176241AGrs10176241211511281.08E-06NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGTHADA
243671904rs6744642TCrs6744642211511281.24E-06NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCTHADA
243721508rs12478601CTrs12478601211511283.00E-23NA1.39[1.30-1.49]744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers12478601-CResearch Support, Non-U.S. Gov'tTTHADA
243721508rs12478601CTrs12478601228859253.37E-10NANANA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTTHADA
243738173rs1038822TCrs1038822211511281.89E-08NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCTHADA
243767039rs7559891GArs7559891211511281.92E-07NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tATHADA
243779665rs1873555TCrs1873555211511283.95E-07NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTTHADA
243781826rs7596052GArs7596052211511281.23E-06NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGTHADA
243782868rs10165527CTrs10165527211511281.90E-06NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTTHADA
243783294rs6726014ATrs6726014211511281.00E-06NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTTHADA
243802380rs2374551CGrs2374551211511282.06E-06NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGTHADA
243803428rs6731009TCrs6731009211511284.94E-07NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTTHADA
243808065rs10179648CTrs10179648211511284.19E-08NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTTHADA
243836687rs7558302CTrs7558302211511286.11E-08NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTNA
248978159rs13405728AGrs13405728211511288.00E-21NA1.41[1.30-1.49]744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers13405728-AResearch Support, Non-U.S. Gov'tALHCGR
248978159rs13405728AGrs13405728228859254.00E-09NA1.35NA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers13405728-AResearch Support, Non-U.S. Gov'tALHCGR
249201612rs2268361CTrs2268361228859251.00E-12NA1.15NA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers2268361-CResearch Support, Non-U.S. Gov'tGFSHR
249247832rs2349415TCrs2349415228859252.35E-12NANANA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCFSHR
249268804rs10865238AGrs10865238228859252.19E-12NANANA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGFSHR
270717507rs3771502AGrs3771502229515950.0000449NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTTGFA
2140220527rs11890914TCrs11890914229515950.0000919NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTNA
2155391135rs2691795CTrs2691795229515950.0000779NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tANA
2209149617rs11678092TGrs11678092229515950.0000374NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTPIKFYVE
389075886rs4555526AGrs4555526221787857.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
3114221822rs7643975CTrs7643975221787858.34E-05Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
4157068139rs11734500ACrs11734500221787854.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
4189498064rs7666129CTrs7666129229515950.0000754NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTLOC401164
582871757rs10514258AGrs10514258211511288.33E-07NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tAVCAN
5131796803rs2706395ATrs2706395229515950.0000486NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTC5orf56
5141721245rs930892GTrs930892221787859.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
5148431964rs36077GArs36077229515950.00000493NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTSH3TC2
5159447213rs10515804AGrs10515804229515950.0000607NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCTTC1
687174156rs9450458CTrs9450458229515950.0000981NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCNA
6124610320rs802500TCrs802500221787856.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
6162169823rs16893004TCrs16893004221787853.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
742209334rs2190513CTrs2190513221787857.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
745167943rs2119050GCrs2119050221787858.91E-05Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
7116285715rs1002399TCrs1002399221787855.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
7116296778rs42476GArs42476221787854.23E-05Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
7116303551rs38833AGrs38833221787857.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
7136690503rs10488602TCrs10488602229515950.00000994NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTCHRM2
7154476131rs7792530GArs7792530229515950.0000753NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGNA
816634751rs971797TGrs971797229515950.0000657NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGNA
870887835rs2044888AGrs2044888229515950.0000941NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGNA
91717031rs10962856AGrs10962856229515950.0000445NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tANA
916185090rs16934192GTrs16934192221787852.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
984308948rs2796441GArs2796441221787852.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
984349621rs2129107TCrs2129107221787853.81E-06Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
997477793rs4744370CTrs4744370228859251.63E-12NANANA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCNA
997648587rs4385527GArs4385527228859255.87E-09NANANA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCC9orf3
997741336rs3802457GArs3802457228859255.00E-14NA1.3NA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers3802457-GResearch Support, Non-U.S. Gov'tCC9orf3
9126446778rs10818854GArs10818854211511289.00E-18NA1.51[1.37-1.65]744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers10818854-AResearch Support, Non-U.S. Gov'tGDENND1A
9126446778rs10818854GArs10818854228859252.50E-04NANANA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGDENND1A
9126507613rs7857605TCrs7857605211511281.33E-07NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTDENND1A
9126525212rs2479106AGrs2479106211511288.00E-19NA1.34[1.26-1.43]744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers2479106-GResearch Support, Non-U.S. Gov'tGDENND1A
9126525212rs2479106AGrs2479106228859255.00E-10NA1.35NA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers2479106-GResearch Support, Non-U.S. Gov'tGDENND1A
9126531755rs1778890TCrs1778890211511282.79E-09NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCDENND1A
9126542704rs1627536ATrs1627536211511283.27E-07NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTDENND1A
9126549955rs10986105TGrs10986105211511286.13E-09NANANA744 Han Chinese cases; 895 Han Chinese controlsHan Chinese(1639)ALL(1639)ASN(1639)ALL(1639)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTDENND1A
9126549955rs10986105TGrs10986105228859251.44E-06NANANA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTDENND1A
9136365146rs28615587TGrs28615587221787852.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
1024600008rs12258036GArs12258036221787855.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
1082288177rs6586051AGrs6586051221787853.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
1082715797rs9988765TCrs9988765229515950.0000682NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCNA
11100435676rs11224282GArs11224282229515950.0000133NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGNA
11102070639rs1894116AGrs1894116228859251.00E-22NA1.27NA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers1894116-GResearch Support, Non-U.S. Gov'tTYAP1
11107053856rs12222308CTrs12222308229515950.000087NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCNA
11116385354rs7952521GArs7952521221787858.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
11119646732rs6589774GArs6589774221787853.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
11126228258rs77137587ATrs77137587221787854.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
11126230844rs77685025GArs77685025221787855.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
11126240911rs78287793AGrs78287793221787855.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
11126263947rs77951192ACrs77951192221787855.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
1221690377rs2417995ACrs2417995229515950.000076NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tAGYS2
1221690774rs10841842ATrs10841842229515950.000076NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tAGYS2
1221691891rs10841843TCrs10841843229515950.0000802NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTGYS2
1221691958rs10492118CTrs10492118229515950.0000971NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCGYS2
1221692949rs1871130AGrs1871130229515950.0000932NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCGYS2
1221693243rs1871129ATrs1871129229515950.0000932NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTGYS2
1221693243rs200581306ATArs1871129229515950.0000932NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTGYS2
1221693244rs1871128TArs1871128229515950.0000932NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tAGYS2
1221699508rs1904121TCrs1904121229515950.0000308NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tAGYS2
1221699916rs6487236GArs6487236229515950.0000697NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tAGYS2
1221699928rs6487237CArs6487237229515950.0000814NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tAGYS2
1221699939rs6487238GArs6487238229515950.0000697NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tAGYS2
1221700495rs7962754TGrs7962754229515950.0000697NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGGYS2
1221701150rs1580300TArs1580300229515950.0000697NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTGYS2
1221701437rs2126885CTrs2126885229515950.0000697NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tAGYS2
1221702005rs7485509CTrs7485509229515950.0000697NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTGYS2
1221702020rs7485489ATrs7485489229515950.0000697NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTGYS2
1221702503rs2169745GCrs2169745229515950.0000697NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGGYS2
1225009856rs11047681GArs11047681229515950.0000511NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGBCAT1
1256364321rs2069408AGrs2069408228859253.73E-17NANANA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tACDK2
1256390636rs705702AGrs705702228859259.00E-26NA1.27NA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers705702-GResearch Support, Non-U.S. Gov'tTNA
1256480583rs877636GArs877636228859253.90E-20NANANA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTERBB3
1256482180rs2292239TGrs2292239228859252.72E-22NANANA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tAERBB3
1266224461rs2272046ACrs2272046228859252.00E-21NA1.43NA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers2272046-AResearch Support, Non-U.S. Gov'tTHMGA2
1266228059rs11175936ACrs11175936229515950.0000521NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tAHMGA2
12110547162rs1547975ACrs1547975221787852.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
12110620661rs7300045CTrs7300045221787852.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
12110757585rs3026465AGrs3026465221787853.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
12110908254rs12369492ACrs12369492221787857.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
12110944299rs61942603GCrs61942603221787857.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
12115459615rs16944877TCrs16944877229515950.0000218NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCNA
1331080015rs9551929AGrs9551929229515950.0000225NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tANA
1380121982rs9545133TCrs9545133221787859.29E-05Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
1394754950rs12428018CTrs12428018221787854.68E-05Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
1478557924rs8020238CTrs8020238221787854.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
1538129204rs1502409TGrs1502409221787852.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
1567438091rs893473AGrs893473221787852.00E-04Polycystic ovary syndromeNANA385 European ancestry cases; 170 European ancestry controlsEuropean(555)ALL(555)EUR(555)ALL(555)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
1586700796rs1867472CTrs1867472229515950.0000848NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tAAGBL1
1652347819rs4784165TGrs4784165228859254.00E-11NA1.15NA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers4784165-GResearch Support, Non-U.S. Gov'tTNA
1652366446rs12927194CTrs12927194229515950.0000838NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCNA
1683078464rs4519324AGrs4519324229515950.0000968NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tACDH13
1687357910rs12918175AGrs12918175229515950.0000441NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tGNA
1862898666rs637644AGrs637644229515950.0000361NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCNA
194554886rs10408176TCrs10408176229515950.000061NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCSEMA6B
197166109rs2059807AGrs2059807228859251.00E-08NA1.14NA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers2059807-GResearch Support, Non-U.S. Gov'tCINSR
1952941171rs1428180TCrs1428180229515950.0000112NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tCZNF534
2052447303rs6022786AGrs6022786228859252.00E-09NA1.13NA2,254 Han Chinese cases; 3,001 Han Chinese controlsHan Chinese(5255)ALL(5255)ASN(5255)ALL(5255)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromers6022786-AResearch Support, Non-U.S. Gov'tANA
2233807636rs7287710TCrs7287710229515950.0000878NANANA774 Korean ancestry cases; 967 Korean ancestry controlsKorean(1741)ALL(1741)ASN(1741)ALL(1741)Polycystic ovary syndromeHPOID:0000147Polycystic ovariesDOID:11612polycystic ovary syndromeD011085Polycystic Ovary SyndromeEFOID:0000660polycystic ovary syndromePolycystic ovary syndromeNAResearch Support, Non-U.S. Gov'tTLARGE
Mapped by lexical matching(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0001939Abnormality of metabolism/homeostasisMP:0020010decreased bone mineral density of femurreduction in the quatitative measurment value of mineral content of bone in the long bone of the thigh
Mapped by homologous gene(Total Items:5)
HP ID HP Name MP ID MP Name Annotation
HP:0000141AmenorrheaMP:0013395eyelid hypoplasiaunderdevelopment or reduced size of the skin folds covering the front of the eyeball, usually due to a decreased cell number
HP:0001007HirsutismMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0001939Abnormality of metabolism/homeostasisMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0000876OligomenorrheaMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0001513ObesityMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
Disease ID 41
Disease polycystic ovary syndrome
Case(Waiting for update.)