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rs875989917

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs875989917(-;-)
Make rs875989917(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11111615
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs875989917
ebirs875989917
HLIrs875989917
Exacrs875989917
Varsomers875989917
Maprs875989917
PheGenIrs875989917
hapmaprs875989917
1000 genomesrs875989917
hgdprs875989917
ensemblrs875989917
gopubmedrs875989917
geneviewrs875989917
scholarrs875989917
googlers875989917
pharmgkbrs875989917
gwascentralrs875989917
openSNPrs875989917
23andMers875989917
23andMe allrs875989917
SNP Nexus

SNPshotrs875989917
SNPdbers875989917
MSV3drs875989917
GWAS Ctlgrs875989917
Max Magnitude0
ClinVar
Risk rs875989917(;)
Alt rs875989917(;)
Reference rs875989917(C;C)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11222291delC
CLNSRC LDLR @ LOVD
CLNACC RCV000211574.2,