TCF7L2, transcription factor 7 like 2, 6934

N. diseases: 257; N. variants: 70
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs290481
rs290481
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE Three SNPs (rs290481, rs290487 and rs290489) located near the 3' end of TCF7L2 gene were associated with HCC risk with marginal significance. 23558246 2013
dbSNP: rs290487
rs290487
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE Three SNPs (rs290481, rs290487 and rs290489) located near the 3' end of TCF7L2 gene were associated with HCC risk with marginal significance. 23558246 2013
dbSNP: rs290489
rs290489
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE Three SNPs (rs290481, rs290487 and rs290489) located near the 3' end of TCF7L2 gene were associated with HCC risk with marginal significance. 23558246 2013