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rs875989887

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs875989887(C;T)
Make rs875989887(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11089409
GeneLDLR
is asnp
is mentioned by
dbSNPrs875989887
ebirs875989887
HLIrs875989887
Exacrs875989887
Varsomers875989887
Maprs875989887
PheGenIrs875989887
hapmaprs875989887
1000 genomesrs875989887
hgdprs875989887
ensemblrs875989887
gopubmedrs875989887
geneviewrs875989887
scholarrs875989887
googlers875989887
pharmgkbrs875989887
gwascentralrs875989887
openSNPrs875989887
23andMers875989887
23andMe allrs875989887
SNP Nexus

SNPshotrs875989887
SNPdbers875989887
MSV3drs875989887
GWAS Ctlgrs875989887
Max Magnitude0
ClinVar
Risk rs875989887(T;T)
Alt rs875989887(T;T)
Reference rs875989887(C;C)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11200085C>G; NC_000019.9:g.11200085C>T
CLNSRC LDLR @ LOVD
CLNACC RCV000237955.1, RCV000211592.2,