Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5063
rs5063
CLCN6 ; NPPA ; NPPA-AS1
0.010 GeneticVariation BEFREE Transition T2238C, which leads to ANP with two additional arginines, and G664A (Val7Met) were investigated with lipid values and clinical phenotype in 83 FH patients. 16721833

2006