Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs879254896
rs879254896
LDLR ; MIR6886
0.010 GeneticVariation BEFREE The A307T mutation did not cosegregate with the clinical phenotype of hypercholesterolemia in the affected family. 9512963

1998