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rs1060500987

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;C) 5 Familial Hypercholesterolemia
(C;C) 0 common in clinvar
Chromosome19
Position11113363
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs1060500987
dbSNP (old)rs1060500987
ClinGenrs1060500987
ebirs1060500987
HLIrs1060500987
Exacrs1060500987
Gnomadrs1060500987
Varsomers1060500987
LitVarrs1060500987
Maprs1060500987
PheGenIrs1060500987
Biobankrs1060500987
1000 genomesrs1060500987
hgdprs1060500987
ensemblrs1060500987
gopubmedrs1060500987
geneviewrs1060500987
scholarrs1060500987
googlers1060500987
pharmgkbrs1060500987
gwascentralrs1060500987
openSNPrs1060500987
23andMers1060500987
23andMe allrs1060500987
SNPshotrs1060500987
SNPdbers1060500987
MSV3drs1060500987
GWAS Ctlgrs1060500987
Max Magnitude5
ClinVar
Risk rs1060500987(-;-)
Alt rs1060500987(-;-)
Reference Rs1060500987(C;C)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11224039delC
CLNSRC
CLNACC RCV000470411.1,