Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs200533979
rs200533979
LDLR ; MIR6886
A 0.700 GeneticVariation CLINVAR Mutational analysis of a cohort with clinical diagnosis of familial hypercholesterolemia: considerations for genetic diagnosis improvement. 26020417

2016