Gene: MIR6886 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs373646964
rs373646964
LDLR ; MIR6886
A 0.700 CausalMutation CLINVAR

dbSNP: rs552422789
rs552422789
LDLR ; MIR6886
A 0.700 CausalMutation CLINVAR

dbSNP: rs570942190
rs570942190
LDLR ; MIR6886
T 0.700 CausalMutation CLINVAR

dbSNP: rs5933
rs5933
LDLR ; MIR6886
G 0.700 CausalMutation CLINVAR

dbSNP: rs730882098
rs730882098
LDLR ; MIR6886
C 0.700 CausalMutation CLINVAR

dbSNP: rs730882103
rs730882103
LDLR ; MIR6886
G 0.700 CausalMutation CLINVAR

dbSNP: rs730882106
rs730882106
LDLR ; MIR6886
T 0.700 CausalMutation CLINVAR

dbSNP: rs745343524
rs745343524
LDLR ; MIR6886
G 0.700 CausalMutation CLINVAR

dbSNP: rs750649426
rs750649426
LDLR ; MIR6886
A 0.700 CausalMutation CLINVAR

dbSNP: rs755667663
rs755667663
LDLR ; MIR6886
T 0.700 CausalMutation CLINVAR

dbSNP: rs765696008
rs765696008
LDLR ; MIR6886
A 0.700 CausalMutation CLINVAR

dbSNP: rs768430352
rs768430352
LDLR ; MIR6886
A 0.700 CausalMutation CLINVAR

dbSNP: rs775924858
rs775924858
LDLR ; MIR6886
A 0.700 CausalMutation CLINVAR

dbSNP: rs778424518
rs778424518
LDLR ; MIR6886
T 0.700 GeneticVariation CLINVAR

dbSNP: rs781362878
rs781362878
LDLR ; MIR6886
A 0.700 GeneticVariation CLINVAR

dbSNP: rs869025453
rs869025453
LDLR ; MIR6886
A 0.700 CausalMutation CLINVAR

dbSNP: rs879254774
rs879254774
LDLR ; MIR6886
A 0.700 CausalMutation CLINVAR

dbSNP: rs879254778
rs879254778
LDLR ; MIR6886
G 0.700 CausalMutation CLINVAR

dbSNP: rs879254781
rs879254781
LDLR ; MIR6886
A 0.700 CausalMutation CLINVAR

dbSNP: rs879254790
rs879254790
LDLR ; MIR6886
GT 0.700 CausalMutation CLINVAR

dbSNP: rs879254791
rs879254791
LDLR ; MIR6886
C 0.700 CausalMutation CLINVAR

dbSNP: rs879254797
rs879254797
LDLR ; MIR6886
A 0.700 CausalMutation CLINVAR

dbSNP: rs879254800
rs879254800
LDLR ; MIR6886
G 0.700 CausalMutation CLINVAR

dbSNP: rs879254805
rs879254805
LDLR ; MIR6886
T 0.700 CausalMutation CLINVAR

dbSNP: rs879254814
rs879254814
LDLR ; MIR6886
C 0.700 CausalMutation CLINVAR