Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894251
rs104894251
KCNJ1
0.010 GeneticVariation BEFREE The HPS phenotype in man can be explained by the lower expression of functional channels by the Kir1.1a[N124K] mutant. 9727001

1998