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rs875989891

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs875989891(A;A)
Make rs875989891(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11102719
GeneLDLR
is asnp
is mentioned by
dbSNPrs875989891
ebirs875989891
HLIrs875989891
Exacrs875989891
Varsomers875989891
Maprs875989891
PheGenIrs875989891
hapmaprs875989891
1000 genomesrs875989891
hgdprs875989891
ensemblrs875989891
gopubmedrs875989891
geneviewrs875989891
scholarrs875989891
googlers875989891
pharmgkbrs875989891
gwascentralrs875989891
openSNPrs875989891
23andMers875989891
23andMe allrs875989891
SNP Nexus

SNPshotrs875989891
SNPdbers875989891
MSV3drs875989891
GWAS Ctlgrs875989891
Max Magnitude0
ClinVar
Risk rs875989891(A;A)
Alt rs875989891(A;A)
Reference rs875989891(C;C)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11213395C>A
CLNSRC LDLR @ LOVD
CLNACC RCV000211576.2,