MIR6886, microRNA 6886, 102465534

N. diseases: 6; N. variants: 286
Disease: Familial hypercholesterolemia - heterozygous ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs879254850
rs879254850
Entrez Id: 3949;102465534
Gene Symbol: LDLR;MIR6886
LDLR;MIR6886
CUI: C0342882
Disease:
Familial hypercholesterolemia - heterozygous 		0.010 GeneticVariation BEFREE Our study indicates that MYLIP p.N342S might be a pharmacogenetic marker for lipid-lowering therapy in patients with FH. 25171759 2014