Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs401681
rs401681
CLPTM1L
0.020 GeneticVariation BEFREE In conclusion, our findings suggest that rs401681 is a possible prognostic biomarker for HCC patients. 29042796

2017
dbSNP: rs401681
rs401681
CLPTM1L
0.020 GeneticVariation BEFREE Both the rs2736098 T allele of TERT and the rs401681 T allele of CLPTM1L were associated with a significantly increased risk of HCC (adjusted odds ratio [OR]=1.605, 95% confidence interval [CI]=1.164-2.213; adjusted OR=1.399, 95%CI=1.002-1.955, respectively). 25339005

2014