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rs875989913

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs875989913(C;T)
Make rs875989913(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11110744
GeneLDLR
is asnp
is mentioned by
dbSNPrs875989913
ebirs875989913
HLIrs875989913
Exacrs875989913
Varsomers875989913
Maprs875989913
PheGenIrs875989913
hapmaprs875989913
1000 genomesrs875989913
hgdprs875989913
ensemblrs875989913
gopubmedrs875989913
geneviewrs875989913
scholarrs875989913
googlers875989913
pharmgkbrs875989913
gwascentralrs875989913
openSNPrs875989913
23andMers875989913
23andMe allrs875989913
SNP Nexus

SNPshotrs875989913
SNPdbers875989913
MSV3drs875989913
GWAS Ctlgrs875989913
Max Magnitude0
ClinVar
Risk rs875989913(T;T)
Alt rs875989913(T;T)
Reference rs875989913(C;C)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11221420C>T
CLNSRC LDLR @ LOVD
CLNACC RCV000211644.2,