Gene: TCF7L2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs290481
rs290481
TCF7L2
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
TCF7L2
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
TCF7L2
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