Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28942078
rs28942078
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		C 0.760 CausalMutation CLINVAR

dbSNP: rs879254842
rs879254842
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		C 0.720 CausalMutation CLINVAR

dbSNP: rs879254918
rs879254918
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		G 0.710 CausalMutation CLINVAR

dbSNP: rs879254851
rs879254851
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		C 0.710 CausalMutation CLINVAR

dbSNP: rs879254850
rs879254850
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		T 0.710 CausalMutation CLINVAR

dbSNP: rs879254814
rs879254814
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		C 0.710 CausalMutation CLINVAR

dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		C 0.710 CausalMutation CLINVAR

dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		A 0.710 CausalMutation CLINVAR

dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		T 0.710 CausalMutation CLINVAR

dbSNP: rs753248521
rs753248521
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		G 0.710 CausalMutation CLINVAR

dbSNP: rs28942080
rs28942080
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		T 0.710 GeneticVariation CLINVAR

dbSNP: rs121908038
rs121908038
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		A 0.710 CausalMutation CLINVAR

dbSNP: rs879254945
rs879254945
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		C 0.700 CausalMutation CLINVAR

dbSNP: rs879254945
rs879254945
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		A 0.700 CausalMutation CLINVAR

dbSNP: rs879254944
rs879254944
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		G 0.700 CausalMutation CLINVAR

dbSNP: rs879254943
rs879254943
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		T 0.700 CausalMutation CLINVAR

dbSNP: rs879254939
rs879254939
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		G 0.700 CausalMutation CLINVAR

dbSNP: rs879254936
rs879254936
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		C 0.700 CausalMutation CLINVAR

dbSNP: rs879254936
rs879254936
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs879254931
rs879254931
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		G 0.700 CausalMutation CLINVAR

dbSNP: rs879254929
rs879254929
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		C 0.700 CausalMutation CLINVAR

dbSNP: rs879254921
rs879254921
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		C 0.700 CausalMutation CLINVAR

dbSNP: rs879254914
rs879254914
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		G 0.700 CausalMutation CLINVAR

dbSNP: rs879254913
rs879254913
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		C 0.700 CausalMutation CLINVAR

dbSNP: rs879254905
rs879254905
LDLR ; MIR6886
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		C 0.700 CausalMutation CLINVAR