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rs878854026

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878854026(C;C)
Make rs878854026(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11100321
GeneLDLR
is asnp
is mentioned by
dbSNPrs878854026
ebirs878854026
HLIrs878854026
Exacrs878854026
Varsomers878854026
Maprs878854026
PheGenIrs878854026
hapmaprs878854026
1000 genomesrs878854026
hgdprs878854026
ensemblrs878854026
gopubmedrs878854026
geneviewrs878854026
scholarrs878854026
googlers878854026
pharmgkbrs878854026
gwascentralrs878854026
openSNPrs878854026
23andMers878854026
23andMe allrs878854026
SNP Nexus

SNPshotrs878854026
SNPdbers878854026
MSV3drs878854026
GWAS Ctlgrs878854026
Max Magnitude0
ClinVar
Risk rs878854026(C;C)
Alt rs878854026(C;C)
Reference rs878854026(T;T)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11210997T>C
CLNSRC LDLR @ LOVD
CLNACC RCV000228737.2,