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rs875989905

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs875989905(-;-)
Make rs875989905(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11105566
GeneLDLR
is asnp
is mentioned by
dbSNPrs875989905
ebirs875989905
HLIrs875989905
Exacrs875989905
Varsomers875989905
Maprs875989905
PheGenIrs875989905
hapmaprs875989905
1000 genomesrs875989905
hgdprs875989905
ensemblrs875989905
gopubmedrs875989905
geneviewrs875989905
scholarrs875989905
googlers875989905
pharmgkbrs875989905
gwascentralrs875989905
openSNPrs875989905
23andMers875989905
23andMe allrs875989905
SNP Nexus

SNPshotrs875989905
SNPdbers875989905
MSV3drs875989905
GWAS Ctlgrs875989905
Max Magnitude0
ClinVar
Risk rs875989905(;)
Alt rs875989905(;)
Reference rs875989905(C;C)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11216242delC
CLNSRC LDLR @ LOVD
CLNACC RCV000211699.2,