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rs875989903

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs875989903(-;-)
Make rs875989903(-;T)
Make rs875989903(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11105554
GeneLDLR
is asnp
is mentioned by
dbSNPrs875989903
ebirs875989903
HLIrs875989903
Exacrs875989903
Varsomers875989903
Maprs875989903
PheGenIrs875989903
hapmaprs875989903
1000 genomesrs875989903
hgdprs875989903
ensemblrs875989903
gopubmedrs875989903
geneviewrs875989903
scholarrs875989903
googlers875989903
pharmgkbrs875989903
gwascentralrs875989903
openSNPrs875989903
23andMers875989903
23andMe allrs875989903
SNP Nexus

SNPshotrs875989903
SNPdbers875989903
MSV3drs875989903
GWAS Ctlgrs875989903
Max Magnitude0
ClinVar
Risk rs875989903(T;T)
Alt rs875989903(T;T)
Reference rs875989903(;)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11216230dupT
CLNSRC LDLR @ LOVD
CLNACC RCV000211601.2,