Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs876657697
rs876657697
LDLR ; MIR6886
GC 0.700 CausalMutation CLINVAR Eight novel LDL receptor gene mutations among patients under LDL apheresis in Dresden and Leipzig. 11139254

2001
dbSNP: rs876657697
rs876657697
LDLR ; MIR6886
GC 0.700 CausalMutation CLINVAR Mutations in the low-density-lipoprotein receptor gene in German patients with familial hypercholesterolaemia. 11196104

2000