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PedAM

Pediatric Disease Annotations & Medicines



   colorectal adenoma
  

Disease ID 581
Disease colorectal adenoma
Definition
An adenoma that arises from the colon or rectum. The group of colorectal adenomas includes tubular, villous, and tubulovillous adenomas, traditional serrated adenomas, sessile serrated adenomas/polyps, and familial adenomatous polyposis.
Synonym
adenoma of large bowel
adenoma of large intestine
adenoma of large intestine (disorder)
adenoma of the large bowel
adenoma of the large intestine
colorectal adenomas
large bowel adenoma
large intestine adenoma
DOID
UMLS
C1302401
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:28)
C1333990  |  lynch syndrome  |  5
C0028754  |  obesity  |  4
C0948265  |  metabolic syndrome  |  4
C0007113  |  rectal cancer  |  3
C0009402  |  colorectal carcinoma  |  3
C0009402  |  colorectal cancer  |  3
C0011847  |  diabetes  |  3
C0007113  |  rectal carcinoma  |  3
C0011849  |  diabetes mellitus  |  2
C0034885  |  rectal neoplasms  |  2
C0032580  |  familial adenomatous polyposis  |  2
C0001430  |  adenoma  |  2
C0032580  |  adenomatous polyposis  |  2
C1140680  |  ovarian ca  |  1
C0011860  |  type 2 diabetes mellitus  |  1
C0006142  |  breast cancer  |  1
C0149925  |  small cell carcinoma  |  1
C0009402  |  colorectal carcinomas  |  1
C0011860  |  type 2 diabetes  |  1
C0149925  |  small cell carcinomas  |  1
C0007570  |  coeliac disease  |  1
C0302592  |  cervical ca  |  1
C1140680  |  ovarian cancer  |  1
C0019196  |  hepatitis c  |  1
C0007847  |  cervical cancer  |  1
C0025149  |  medulloblastoma  |  1
C0271650  |  prediabetes  |  1
C0019158  |  hepatitis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
APC  |  324  |  CLINVAR
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:18)
4548  |  MTR  |  infer
5243  |  ABCB1  |  infer
324  |  APC  |  infer
8313  |  AXIN2  |  infer
581  |  BAX  |  infer
1499  |  CTNNB1  |  infer
3265  |  HRAS  |  infer
4292  |  MLH1  |  infer
4436  |  MSH2  |  infer
4619  |  MYH1  |  infer
9  |  NAT1  |  infer
64127  |  NOD2  |  infer
6555  |  SLC10A2  |  infer
7048  |  TGFBR2  |  infer
7157  |  TP53  |  infer
7298  |  TYMS  |  infer
54658  |  UGT1A1  |  infer
7421  |  VDR  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:249)
400500  |  BCAR4  |  DISEASES
643911  |  CRNDE  |  DISEASES
6542  |  SLC7A2  |  DISEASES
54474  |  KRT20  |  DISEASES
7022  |  TFAP2C  |  DISEASES
151887  |  CCDC80  |  DISEASES
4320  |  MMP11  |  DISEASES
328  |  APEX1  |  DISEASES
1591  |  CYP24A1  |  DISEASES
6790  |  AURKA  |  DISEASES
25878  |  MXRA5  |  DISEASES
10562  |  OLFM4  |  DISEASES
4913  |  NTHL1  |  DISEASES
6422  |  SFRP1  |  DISEASES
7991  |  TUSC3  |  DISEASES
56729  |  RETN  |  DISEASES
6449  |  SGTA  |  DISEASES
1048  |  CEACAM5  |  DISEASES
7980  |  TFPI2  |  DISEASES
10135  |  NAMPT  |  DISEASES
6372  |  CXCL6  |  DISEASES
595  |  CCND1  |  DISEASES
1594  |  CYP27B1  |  DISEASES
84519  |  ACRBP  |  DISEASES
4292  |  MLH1  |  DISEASES
10641  |  NPRL2  |  DISEASES
4436  |  MSH2  |  DISEASES
7475  |  WNT6  |  DISEASES
4953  |  ODC1  |  DISEASES
607  |  BCL9  |  DISEASES
60672  |  MIIP  |  DISEASES
1509  |  CTSD  |  DISEASES
7976  |  FZD3  |  DISEASES
92  |  ACVR2A  |  DISEASES
7291  |  TWIST1  |  DISEASES
2952  |  GSTT1  |  DISEASES
50833  |  TAS2R16  |  DISEASES
1036  |  CDO1  |  DISEASES
3630  |  INS  |  DISEASES
239  |  ALOX12  |  DISEASES
50484  |  RRM2B  |  DISEASES
9518  |  GDF15  |  DISEASES
11047  |  ADRM1  |  DISEASES
9584  |  RBM39  |  DISEASES
1401  |  CRP  |  DISEASES
3845  |  KRAS  |  DISEASES
83998  |  REG4  |  DISEASES
2947  |  GSTM3  |  DISEASES
902  |  CCNH  |  DISEASES
8933  |  FAM127A  |  DISEASES
3569  |  IL6  |  DISEASES
4316  |  MMP7  |  DISEASES
109  |  ADCY3  |  DISEASES
1559  |  CYP2C9  |  DISEASES
490  |  ATP2B1  |  DISEASES
1800  |  DPEP1  |  DISEASES
217  |  ALDH2  |  DISEASES
999  |  CDH1  |  DISEASES
7515  |  XRCC1  |  DISEASES
1434  |  CSE1L  |  DISEASES
25927  |  CNRIP1  |  DISEASES
79968  |  WDR76  |  DISEASES
658  |  BMPR1B  |  DISEASES
55247  |  NEIL3  |  DISEASES
4552  |  MTRR  |  DISEASES
306  |  ANXA3  |  DISEASES
55573  |  CDV3  |  DISEASES
10923  |  SUB1  |  DISEASES
64374  |  SIL1  |  DISEASES
320  |  APBA1  |  DISEASES
27074  |  LAMP3  |  DISEASES
11083  |  DIDO1  |  DISEASES
24148  |  PRPF6  |  DISEASES
8549  |  LGR5  |  DISEASES
6652  |  SORD  |  DISEASES
7157  |  TP53  |  DISEASES
2064  |  ERBB2  |  DISEASES
57410  |  SCYL1  |  DISEASES
6282  |  S100A11  |  DISEASES
2052  |  EPHX1  |  DISEASES
6423  |  SFRP2  |  DISEASES
635  |  BHMT  |  DISEASES
3484  |  IGFBP1  |  DISEASES
3934  |  LCN2  |  DISEASES
288  |  ANK3  |  DISEASES
252969  |  NEIL2  |  DISEASES
7476  |  WNT7A  |  DISEASES
27123  |  DKK2  |  DISEASES
114  |  ADCY8  |  DISEASES
10  |  NAT2  |  DISEASES
11197  |  WIF1  |  DISEASES
9073  |  CLDN8  |  DISEASES
7832  |  BTG2  |  DISEASES
8888  |  MCM3AP  |  DISEASES
10197  |  PSME3  |  DISEASES
128  |  ADH5  |  DISEASES
3015  |  H2AFZ  |  DISEASES
3248  |  HPGD  |  DISEASES
85477  |  SCIN  |  DISEASES
81693  |  AMN  |  DISEASES
9318  |  COPS2  |  DISEASES
26585  |  GREM1  |  DISEASES
9780  |  PIEZO1  |  DISEASES
1581  |  CYP7A1  |  DISEASES
4255  |  MGMT  |  DISEASES
3479  |  IGF1  |  DISEASES
9963  |  SLC23A1  |  DISEASES
347169  |  OR1B1  |  DISEASES
54578  |  UGT1A6  |  DISEASES
5729  |  PTGDR  |  DISEASES
7764  |  ZNF217  |  DISEASES
54463  |  FAM134B  |  DISEASES
4968  |  OGG1  |  DISEASES
125  |  ADH1B  |  DISEASES
6573  |  SLC19A1  |  DISEASES
6596  |  HLTF  |  DISEASES
3265  |  HRAS  |  DISEASES
2829  |  XCR1  |  DISEASES
836  |  CASP3  |  DISEASES
2944  |  GSTM1  |  DISEASES
3952  |  LEP  |  DISEASES
341208  |  HEPHL1  |  DISEASES
163  |  AP2B1  |  DISEASES
7298  |  TYMS  |  DISEASES
65059  |  RAPH1  |  DISEASES
10170  |  DHRS9  |  DISEASES
115207  |  KCTD12  |  DISEASES
55603  |  FAM46A  |  DISEASES
10808  |  HSPH1  |  DISEASES
221150  |  SKA3  |  DISEASES
1728  |  NQO1  |  DISEASES
5315  |  PKM  |  DISEASES
114876  |  OSBPL1A  |  DISEASES
9370  |  ADIPOQ  |  DISEASES
6817  |  SULT1A1  |  DISEASES
84289  |  ING5  |  DISEASES
7284  |  TUFM  |  DISEASES
4312  |  MMP1  |  DISEASES
1789  |  DNMT3B  |  DISEASES
22906  |  TRAK1  |  DISEASES
54059  |  YBEY  |  DISEASES
3953  |  LEPR  |  DISEASES
6938  |  TCF12  |  DISEASES
2520  |  GAST  |  DISEASES
5797  |  PTPRM  |  DISEASES
6546  |  SLC8A1  |  DISEASES
10732  |  TCFL5  |  DISEASES
120227  |  CYP2R1  |  DISEASES
2938  |  GSTA1  |  DISEASES
1984  |  EIF5A  |  DISEASES
3091  |  HIF1A  |  DISEASES
7360  |  UGP2  |  DISEASES
1429  |  CRYZ  |  DISEASES
63826  |  SRR  |  DISEASES
55969  |  C20orf24  |  DISEASES
27255  |  CNTN6  |  DISEASES
1544  |  CYP1A2  |  DISEASES
1508  |  CTSB  |  DISEASES
2272  |  FHIT  |  DISEASES
10620  |  ARID3B  |  DISEASES
7517  |  XRCC3  |  DISEASES
7464  |  CORO2A  |  DISEASES
27068  |  PPA2  |  DISEASES
54914  |  FOCAD  |  DISEASES
9962  |  SLC23A2  |  DISEASES
1499  |  CTNNB1  |  DISEASES
80142  |  PTGES2  |  DISEASES
10541  |  ANP32B  |  DISEASES
54600  |  UGT1A9  |  DISEASES
79661  |  NEIL1  |  DISEASES
23111  |  SPG20  |  DISEASES
2204  |  FCAR  |  DISEASES
51703  |  ACSL5  |  DISEASES
55544  |  RBM38  |  DISEASES
122786  |  FRMD6  |  DISEASES
10616  |  RBCK1  |  DISEASES
5887  |  RAD23B  |  DISEASES
54879  |  ST7L  |  DISEASES
1612  |  DAPK1  |  DISEASES
1510  |  CTSE  |  DISEASES
489  |  ATP2A3  |  DISEASES
7169  |  TPM2  |  DISEASES
5742  |  PTGS1  |  DISEASES
4548  |  MTR  |  DISEASES
5743  |  PTGS2  |  DISEASES
9095  |  TBX19  |  DISEASES
4582  |  MUC1  |  DISEASES
63910  |  SLC17A9  |  DISEASES
55257  |  MRGBP  |  DISEASES
1791  |  DNTT  |  DISEASES
7422  |  VEGFA  |  DISEASES
4595  |  MUTYH  |  DISEASES
57158  |  JPH2  |  DISEASES
5464  |  PPA1  |  DISEASES
54577  |  UGT1A7  |  DISEASES
79980  |  DSN1  |  DISEASES
23013  |  SPEN  |  DISEASES
29968  |  PSAT1  |  DISEASES
4524  |  MTHFR  |  DISEASES
22894  |  DIS3  |  DISEASES
9770  |  RASSF2  |  DISEASES
7905  |  REEP5  |  DISEASES
1543  |  CYP1A1  |  DISEASES
81567  |  TXNDC5  |  DISEASES
5209  |  PFKFB3  |  DISEASES
4507  |  MTAP  |  DISEASES
150084  |  IGSF5  |  DISEASES
1045  |  CDX2  |  DISEASES
3486  |  IGFBP3  |  DISEASES
10171  |  RCL1  |  DISEASES
23600  |  AMACR  |  DISEASES
5268  |  SERPINB5  |  DISEASES
2878  |  GPX3  |  DISEASES
284217  |  LAMA1  |  DISEASES
23143  |  LRCH1  |  DISEASES
80196  |  RNF34  |  DISEASES
145270  |  PRIMA1  |  DISEASES
10265  |  IRX5  |  DISEASES
5239  |  PGM5  |  DISEASES
4689  |  NCF4  |  DISEASES
81502  |  HM13  |  DISEASES
2950  |  GSTP1  |  DISEASES
125150  |  ZSWIM7  |  DISEASES
387267  |  KRTAP5-4  |  DISEASES
51701  |  NLK  |  DISEASES
54894  |  RNF43  |  DISEASES
55083  |  KIF26B  |  DISEASES
1630  |  DCC  |  DISEASES
3481  |  IGF2  |  DISEASES
1029  |  CDKN2A  |  DISEASES
960  |  CD44  |  DISEASES
7124  |  TNF  |  DISEASES
5424  |  POLD1  |  DISEASES
10015  |  PDCD6IP  |  DISEASES
3586  |  IL10  |  DISEASES
4583  |  MUC2  |  DISEASES
8125  |  ANP32A  |  DISEASES
846  |  CASR  |  DISEASES
573  |  BAG1  |  DISEASES
259296  |  TAS2R50  |  DISEASES
9788  |  MTSS1  |  DISEASES
4008  |  LMO7  |  DISEASES
91  |  ACVR1B  |  DISEASES
9  |  NAT1  |  DISEASES
7421  |  VDR  |  DISEASES
5726  |  TAS2R38  |  DISEASES
321  |  APBA2  |  DISEASES
378805  |  LINC-PINT  |  DISEASES
26801  |  SNORD48  |  DISEASES
Locus(Waiting for update.)
Disease ID 581
Disease colorectal adenoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:11)
HP:0030731  |  Carcinoma  |  6
HP:0001513  |  Obesity  |  4
HP:0002664  |  Neoplasia  |  3
HP:0000855  |  Insulin resistance  |  2
HP:0000819  |  Diabetes mellitus  |  2
HP:0002885  |  Medulloblastoma  |  1
HP:0005231  |  Chronic gastritis  |  1
HP:0001717  |  Coronary artery calcification  |  1
HP:0003002  |  Breast carcinoma  |  1
HP:0012115  |  Liver inflammation  |  1
HP:0001397  |  Hepatic steatosis  |  1
Disease ID 581
Disease colorectal adenoma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:7)
C1608408  |  malignant transformation
C1527249  |  colorectal cancer
C1518171  |  malignant conversion
C0878500  |  intraepithelial neoplasia
C0878500  |  epithelial dysplasia
C0029440  |  osteomas
C0007099  |  carcinoma in situ
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:2)
C0009402  |  colorectal cancer  |  3
C1518171  |  malignant conversion  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:43)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1051740215981782052EPHX1umls:C1302401BeFreeWe determined the association between charred meat consumption, cigarette smoking, microsomal epoxide hydrolase (mEH) polymorphisms (rs1051740 and rs2234922), and colorectal adenomas and hyperplastic polyps (HPs) and explored gene-environment interactions.0.0013572092011EPHX11225831932TC
rs1052133159467954968OGG1umls:C1302401BeFreeGPX Pro198Leu and OGG1 Ser326Cys polymorphisms and risk of development of colorectal adenomas and colorectal cancer.0.0008143262005OGG1;CAMK139757089CG
rs112666717236225239ALOX12umls:C1302401BeFreeHowever, there was an inverse association between the Arg261Gln polymorphism in 12-LOX and colorectal adenoma (OR, 0.63; 95% CI, 0.40-1.00).0.0002714422007ALOX12;ALOX12-AS1176999441AG
rs1138272221611382944GSTM1umls:C1302401BeFreeAlthough with modest limitations and biases, this metaanalysis suggests that EPHX1 Tyr113His and His139Arg, GSTT1, GSTM1, GSTP1 Ile105Val and Ala114Val polymorphisms may be not risk factors for CRA development, while Ser allele of NQO1 Ser187 Pro may be a modest risk factor for CRA development, and may be used with other genetic markers for screening CRA in the future.0.0027144192012GSTP11167586108CT
rs1138272221611382950GSTP1umls:C1302401BeFreeAlthough with modest limitations and biases, this metaanalysis suggests that EPHX1 Tyr113His and His139Arg, GSTT1, GSTM1, GSTP1 Ile105Val and Ala114Val polymorphisms may be not risk factors for CRA development, while Ser allele of NQO1 Ser187 Pro may be a modest risk factor for CRA development, and may be used with other genetic markers for screening CRA in the future.0.0008143262012GSTP11167586108CT
rs1138272221611381728NQO1umls:C1302401BeFreeAlthough with modest limitations and biases, this metaanalysis suggests that EPHX1 Tyr113His and His139Arg, GSTT1, GSTM1, GSTP1 Ile105Val and Ala114Val polymorphisms may be not risk factors for CRA development, while Ser allele of NQO1 Ser187 Pro may be a modest risk factor for CRA development, and may be used with other genetic markers for screening CRA in the future.0.0013572092012GSTP11167586108CT
rs138367627NA324APCumls:C1302401CLINVARNA0.139391925NAAPC5112840326TG
rs1695221611381728NQO1umls:C1302401BeFreeAlthough with modest limitations and biases, this metaanalysis suggests that EPHX1 Tyr113His and His139Arg, GSTT1, GSTM1, GSTP1 Ile105Val and Ala114Val polymorphisms may be not risk factors for CRA development, while Ser allele of NQO1 Ser187 Pro may be a modest risk factor for CRA development, and may be used with other genetic markers for screening CRA in the future.0.0013572092012GSTP11167585218AG
rs1695221611382944GSTM1umls:C1302401BeFreeAlthough with modest limitations and biases, this metaanalysis suggests that EPHX1 Tyr113His and His139Arg, GSTT1, GSTM1, GSTP1 Ile105Val and Ala114Val polymorphisms may be not risk factors for CRA development, while Ser allele of NQO1 Ser187 Pro may be a modest risk factor for CRA development, and may be used with other genetic markers for screening CRA in the future.0.0027144192012GSTP11167585218AG
rs1695221611382950GSTP1umls:C1302401BeFreeAlthough with modest limitations and biases, this metaanalysis suggests that EPHX1 Tyr113His and His139Arg, GSTT1, GSTM1, GSTP1 Ile105Val and Ala114Val polymorphisms may be not risk factors for CRA development, while Ser allele of NQO1 Ser187 Pro may be a modest risk factor for CRA development, and may be used with other genetic markers for screening CRA in the future.0.0008143262012GSTP11167585218AG
rs1799782157673384233METumls:C1302401BeFreeUsing a large sigmoidoscopy-based case-control study (753 cases and 799 controls) in Los Angeles County, we investigated possible associations between single-nucleotide polymorphisms in the XRCC1 (codons 194 Arg/Trp and codon 399 Arg/Gln) and XRCC3 (codon 241 Thr/Met) genes and colorectal adenoma risk and their possible role as modifiers of the effect of monounsaturated fatty acid, the ratio of omega-6/omega-3 polyunsaturated fatty acids, and antioxidant intake.0.0008143262005XRCC11943553422GA
rs1800566221611381728NQO1umls:C1302401BeFreeAlthough with modest limitations and biases, this metaanalysis suggests that EPHX1 Tyr113His and His139Arg, GSTT1, GSTM1, GSTP1 Ile105Val and Ala114Val polymorphisms may be not risk factors for CRA development, while Ser allele of NQO1 Ser187 Pro may be a modest risk factor for CRA development, and may be used with other genetic markers for screening CRA in the future.0.0013572092012NQO11669711242GA
rs1800566221611382950GSTP1umls:C1302401BeFreeAlthough with modest limitations and biases, this metaanalysis suggests that EPHX1 Tyr113His and His139Arg, GSTT1, GSTM1, GSTP1 Ile105Val and Ala114Val polymorphisms may be not risk factors for CRA development, while Ser allele of NQO1 Ser187 Pro may be a modest risk factor for CRA development, and may be used with other genetic markers for screening CRA in the future.0.0008143262012NQO11669711242GA
rs1800566223062491728NQO1umls:C1302401BeFreeContribution of NAD(P)H quinone oxidoreductase 1 (NQO1) Pro187Ser polymorphism and risk of colorectal adenoma and colorectal cancer in Caucasians: a meta-analysis.0.0013572092012NQO11669711242GA
rs1800566221611382944GSTM1umls:C1302401BeFreeAlthough with modest limitations and biases, this metaanalysis suggests that EPHX1 Tyr113His and His139Arg, GSTT1, GSTM1, GSTP1 Ile105Val and Ala114Val polymorphisms may be not risk factors for CRA development, while Ser allele of NQO1 Ser187 Pro may be a modest risk factor for CRA development, and may be used with other genetic markers for screening CRA in the future.0.0027144192012NQO11669711242GA
rs180115515266213324APCumls:C1302401BeFreeThe APC I1307K and E1317Q variants predispose to colorectal adenomas and carcinomas in Caucasians, but data are lacking in Asians.0.1393919252004APC5112839514TA
rs180116619701947324APCumls:C1302401BeFreeThe APC Variant p.Glu1317Gln predisposes to colorectal adenomas by a novel mechanism of relaxing the target for tumorigenic somatic APC mutations.0.1393919252009APC5112839543GC
rs180116619474113324APCumls:C1302401BeFreeThe APC E1317Q variant is associated with colorectal neoplasia, particularly colorectal adenomas, but further studies are still needed.0.1393919252009APC5112839543GC
rs180116615266213324APCumls:C1302401BeFreeThe APC I1307K and E1317Q variants predispose to colorectal adenomas and carcinomas in Caucasians, but data are lacking in Asians.0.1393919252004APC5112839543GC
rs180116611001924324APCumls:C1302401BeFreeGermline APC variants in patients with multiple colorectal adenomas, with evidence for the particular importance of E1317Q.0.1393919252000APC5112839543GC
rs180116612537656324APCumls:C1302401BeFreePrevalence of the E1317Q variant of the APC gene in Italian patients with colorectal adenomas.0.1393919252002APC5112839543GC
rs1801282155642895468PPARGumls:C1302401BeFreeLarger studies are needed to validate these results, which suggest that the PPARgamma Pro12Ala polymorphism may interact with other factors to protect against colorectal adenoma.0.0008143262005PPARG312351626CG
rs1805087147447494548MTRumls:C1302401BeFreeMethionine synthase D919G polymorphism, folate metabolism, and colorectal adenoma risk.0.0037242412004MTR1236885200AG
rs1805087191245084548MTRumls:C1302401BeFreeMethionine synthase A2756G polymorphism interacts with alcohol and folate intake to influence the risk of colorectal adenoma.0.0037242412009MTR1236885200AG
rs1805087235932294548MTRumls:C1302401BeFreeMethionine synthase A2756G polymorphism and risk of colorectal adenoma and cancer: evidence based on 27 studies.0.0037242412013MTR1236885200AG
rs1805192155642895468PPARGumls:C1302401BeFreeLarger studies are needed to validate these results, which suggest that the PPARgamma Pro12Ala polymorphism may interact with other factors to protect against colorectal adenoma.0.0008143262005PPARG312379739CG
rs188096186441226555SLC10A2umls:C1302401BeFreeRecently, an association of colorectal adenoma with two variants (c.507C>T;p.L169L and c.511G>T;p.A171S) of the ileal sodium dependent bile acid transporter gene (SLC10A2) has been reported.0.0029099162008SLC10A213103052694AC
rs1979277171132246470SHMT1umls:C1302401BeFreeIn a case-control study, including 768 cases and 709 controls, we investigated the associations between colorectal adenomas and TS tandem repeat and SHMT1 C1420T polymorphisms, and the interplay with B-vitamins.0.0002714422007SHMT11718328782GA
rs2234922215981782052EPHX1umls:C1302401BeFreeWe determined the association between charred meat consumption, cigarette smoking, microsomal epoxide hydrolase (mEH) polymorphisms (rs1051740 and rs2234922), and colorectal adenomas and hyperplastic polyps (HPs) and explored gene-environment interactions.0.0013572092011EPHX11225838705AG,T
rs2287780173896184552MTRRumls:C1302401BeFreeIn addition, the methionine synthase reductase (MTRR) Arg415Cys and MTRR Ser284Thr variant carriers, also in the vitamin B(12) pathway, have suggestive associations with advanced colorectal adenoma (defined as being larger than 1 cm, villous, tubular-villous or carcinoma in situ histology).0.0002714422007MTRR57889191CT
rs2303080173896184552MTRRumls:C1302401BeFreeIn addition, the methionine synthase reductase (MTRR) Arg415Cys and MTRR Ser284Thr variant carriers, also in the vitamin B(12) pathway, have suggestive associations with advanced colorectal adenoma (defined as being larger than 1 cm, villous, tubular-villous or carcinoma in situ histology).0.0002714422007MTRR57878311TA
rs25487157673384233METumls:C1302401BeFreeUsing a large sigmoidoscopy-based case-control study (753 cases and 799 controls) in Los Angeles County, we investigated possible associations between single-nucleotide polymorphisms in the XRCC1 (codons 194 Arg/Trp and codon 399 Arg/Gln) and XRCC3 (codon 241 Thr/Met) genes and colorectal adenoma risk and their possible role as modifiers of the effect of monounsaturated fatty acid, the ratio of omega-6/omega-3 polyunsaturated fatty acids, and antioxidant intake.0.0008143262005XRCC11943551574TC
rs288326190671932487FRZBumls:C1302401BeFreeTo determine if this finding could be replicated, we investigated the association between two FRZB polymorphisms (Arg324Gly and Arg200Trp) and the risk of colorectal adenoma and cancer in nested case-control studies.0.0002714422009FRZB2182838608GA
rs371085910NA324APCumls:C1302401CLINVARNA0.139391925NAAPC5112775655AG
rs373389017389618635BHMTumls:C1302401BeFreeWe observed significant evidence for departure from multiplicative interaction for the betaine-homocysteine methyltransferase (BHMT) Arg239Gln with dietary methyl status (based on intake of dietary folate, methionine and alcohol intake) in relation to colorectal adenoma; no such interaction was observed for the other 23 SNPs.0.0002714422007BHMT579126136GA
rs386493716157673384233METumls:C1302401BeFreeUsing a large sigmoidoscopy-based case-control study (753 cases and 799 controls) in Los Angeles County, we investigated possible associations between single-nucleotide polymorphisms in the XRCC1 (codons 194 Arg/Trp and codon 399 Arg/Gln) and XRCC3 (codon 241 Thr/Met) genes and colorectal adenoma risk and their possible role as modifiers of the effect of monounsaturated fatty acid, the ratio of omega-6/omega-3 polyunsaturated fatty acids, and antioxidant intake.0.0008143262005NANANANANA
rs386545546157673384233METumls:C1302401BeFreeUsing a large sigmoidoscopy-based case-control study (753 cases and 799 controls) in Los Angeles County, we investigated possible associations between single-nucleotide polymorphisms in the XRCC1 (codons 194 Arg/Trp and codon 399 Arg/Gln) and XRCC3 (codon 241 Thr/Met) genes and colorectal adenoma risk and their possible role as modifiers of the effect of monounsaturated fatty acid, the ratio of omega-6/omega-3 polyunsaturated fatty acids, and antioxidant intake.0.0008143262005NANANANANA
rs397507444167836074524MTHFRumls:C1302401BeFreeMTHFR (C677T and A1298C) polymorphisms and risk of sporadic distal colorectal adenoma in the UK Flexible Sigmoidoscopy Screening Trial (United Kingdom).0.004343072006MTHFR111794407TG
rs397507444170890704524MTHFRumls:C1302401BeFreeDifferent roles of MTHFR C677T and A1298C polymorphisms in colorectal adenoma and colorectal cancer: a meta-analysis.0.004343072007MTHFR111794407TG
rs397507444170879564524MTHFRumls:C1302401BeFreeWe assessed 2 polymorphisms in the MTHFR gene (C677T and A1298C) in relation to colorectal adenoma recurrence and conducted analyses to investigate their joint effects with plasma and dietary markers of folate status.0.004343072006MTHFR111794407TG
rs41281678186441226555SLC10A2umls:C1302401BeFreeRecently, an association of colorectal adenoma with two variants (c.507C>T;p.L169L and c.511G>T;p.A171S) of the ileal sodium dependent bile acid transporter gene (SLC10A2) has been reported.0.0029099162008SLC10A213103052700GA
rs7023329233610494507MTAPumls:C1302401BeFreeOne SNP in MTAP (methylthioadenosine phosphorylase) (rs7023329) that was previously associated with melanoma and nevi in multiple genome-wide association studies was associated with CRC, CA and OS by ASSET (P=0.007).0.0002714422013MTAP921816529AG
rs7775190671932487FRZBumls:C1302401BeFreeTo determine if this finding could be replicated, we investigated the association between two FRZB polymorphisms (Arg324Gly and Arg200Trp) and the risk of colorectal adenoma and cancer in nested case-control studies.0.0002714422009FRZB2182834857GT,C,A
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