Gene: HSD17B13 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72613567
rs72613567
HSD17B13
0.030 GeneticVariation BEFREE A common loss-of-function variant in HSD17B13 (rs72613567:TA) was recently found to protect from chronic liver disease. 31155741

2020
dbSNP: rs72613567
rs72613567
HSD17B13
0.030 GeneticVariation BEFREE A recent study identified a common SNP in HSD17B13 (rs72613567) that conferred protection from chronic liver disease. 31517326

2019
dbSNP: rs72613567
rs72613567
HSD17B13
0.030 GeneticVariation BEFREE A total of 3,315 European patients with HCC (n = 1,109) or without HCC, but with chronic liver disease (CLD; n = 2,206), from four centers were analyzed either by whole-exome sequencing (WES; exploratory cohort, 285 HCC) or genotyped for HSD17B13 rs72613567 (validation cohort, 824 HCC and all CLD). 30908678

2019