Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7763881
rs7763881
Entrez Id: 728655;100506207
Gene Symbol: HULC;LOC100506207
HULC;LOC100506207
CUI: C2239176
Disease:
Liver carcinoma
0.020 GeneticVariation BEFREE HULC rs7763881 AC/CC genotype was significantly associated with decreased HCC risk. 31009106 2019
dbSNP: rs7763881
rs7763881
Entrez Id: 728655;100506207
Gene Symbol: HULC;LOC100506207
HULC;LOC100506207
CUI: C2239176
Disease:
Liver carcinoma
0.020 GeneticVariation BEFREE The variant genotypes of rs7763881 in HULC may contribute to decreased susceptibility to HCC in HBV persistent carriers. 22493738 2012