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rs6585194

From SNPedia

Orientationplus
Stabilizedplus
Make rs6585194(C;C)
Make rs6585194(C;G)
Make rs6585194(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position112957712
GeneTCF7L2
is asnp
is mentioned by
dbSNPrs6585194
ebirs6585194
HLIrs6585194
Exacrs6585194
Varsomers6585194
Maprs6585194
PheGenIrs6585194
hapmaprs6585194
1000 genomesrs6585194
hgdprs6585194
ensemblrs6585194
gopubmedrs6585194
geneviewrs6585194
scholarrs6585194
googlers6585194
pharmgkbrs6585194
gwascentralrs6585194
openSNPrs6585194
23andMers6585194
23andMe allrs6585194
SNP Nexus

SNPshotrs6585194
SNPdbers6585194
MSV3drs6585194
GWAS Ctlgrs6585194
GMAF0.3613
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 23558246] Impacts of TCF7L2 gene polymorphisms on the susceptibility of hepatogenous diabetes and hepatocellular carcinoma in cirrhotic patients [PMID 19351735OA-icon.png] Evidence for association between polycystic ovary syndrome (PCOS) and TCF7L2 and glucose intolerance in women with PCOS and TCF7L2.