Have questions? Visit https://www.reddit.com/r/SNPedia

rs3814570

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 1 Normal risk of developing Crohn's disease
(C;T) 1.5 1.3x increased risk for Crohn's disease with ileal involvement
(T;T) 1.5 1.3x increased risk for Crohn's disease with ileal involvement
ReferenceGRCh38 38.1/142
Chromosome10
Position112948751
GeneTCF7L2
is asnp
is mentioned by
dbSNPrs3814570
dbSNP (classic)rs3814570
ClinGenrs3814570
ebirs3814570
HLIrs3814570
Exacrs3814570
Gnomadrs3814570
Varsomers3814570
LitVarrs3814570
Maprs3814570
PheGenIrs3814570
Biobankrs3814570
1000 genomesrs3814570
hgdprs3814570
ensemblrs3814570
geneviewrs3814570
scholarrs3814570
googlers3814570
pharmgkbrs3814570
gwascentralrs3814570
openSNPrs3814570
23andMers3814570
SNPshotrs3814570
SNPdbers3814570
MSV3drs3814570
GWAS Ctlgrs3814570
GMAF0.1818
Max Magnitude1.5
? (C;C) (C;T) (T;T) 28


rs3814570 is a SNP in the transcription factor 7-like 2 (T-cell specific, HMG-box) TCF7L2 gene.

A study of 784 Crohn's disease patients with ileal involvement concluded that rs3814570 was associated with increased risk, but not with risk for colonic Crohn's disease or ulcerative colitis. The odds ratio was 1.27 (CI: 1.07 - 1.52, p = 0.00737).[PMID 19221600OA-icon.png]

[PMID 19351735OA-icon.png] Evidence for association between polycystic ovary syndrome (PCOS) and TCF7L2 and glucose intolerance in women with PCOS and TCF7L2.