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rs875989923

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs875989923(A;A)
Make rs875989923(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11113731
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs875989923
ebirs875989923
HLIrs875989923
Exacrs875989923
Varsomers875989923
Maprs875989923
PheGenIrs875989923
hapmaprs875989923
1000 genomesrs875989923
hgdprs875989923
ensemblrs875989923
gopubmedrs875989923
geneviewrs875989923
scholarrs875989923
googlers875989923
pharmgkbrs875989923
gwascentralrs875989923
openSNPrs875989923
23andMers875989923
23andMe allrs875989923
SNP Nexus

SNPshotrs875989923
SNPdbers875989923
MSV3drs875989923
GWAS Ctlgrs875989923
Max Magnitude0
ClinVar
Risk rs875989923(A;A)
Alt rs875989923(A;A)
Reference rs875989923(C;C)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11224407C>A; NC_000019.9:g.11224407C>T
CLNSRC LDLR @ LOVD
CLNACC RCV000211565.1, RCV000237344.1,