Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852912
rs137852912
0.740 GeneticVariation BEFREE We have hypothesized that transgenic Ossabaw swine expressing chimp <i>PCSK9</i> (proprotein convertase subtilisin-like/kexin type 9) containing the D374Y gain of function would develop familial hypercholesterolemia and coronary artery plaques more rapidly than Landrace swine with the same transgene. 29572319

2018

dbSNP: rs137852912
rs137852912
0.740 GeneticVariation BEFREE PCSK 9 gain-of-function mutations (R496W and D374Y) and clinical cardiovascular characteristics in a cohort of Turkish patients with familial hypercholesterolemia. 28777095

2017

dbSNP: rs137852912
rs137852912
0.740 GeneticVariation BEFREE We measured plasma PCSK9 concentrations in healthy men with a PCSK9 (proprotein convertase subtilisin/kexin type 9) loss-of-function variant (p.R46L), in statin-treated patients with a clinical diagnosis of familial hypercholesterolemia (FH) and carrying a PCSK9 gain-of-function mutation (p.D374Y), and in statin-treated patients with FH due to different genetic causes. 19797716

2009

dbSNP: rs137852912
rs137852912
0.740 GeneticVariation BEFREE We have identified the D374Y mutant of PCSK9 in three FH families of English origin; all 12 affected individuals have unusually severe hypercholesterolaemia and require more stringent treatment than typical FH patients, who are heterozygous for defects in the LDL receptor. 15772090

2005

dbSNP: rs137852912
rs137852912
C 0.740 CausalMutation CLINVAR

dbSNP: rs137852912
rs137852912
T 0.740 GeneticVariation CLINVAR

dbSNP: rs137852912
rs137852912
T 0.740 CausalMutation CLINVAR