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rs758927662

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs758927662(G;G)
Make rs758927662(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11102698
GeneLDLR
is asnp
is mentioned by
dbSNPrs758927662
ebirs758927662
HLIrs758927662
Exacrs758927662
Varsomers758927662
Maprs758927662
PheGenIrs758927662
hapmaprs758927662
1000 genomesrs758927662
hgdprs758927662
ensemblrs758927662
gopubmedrs758927662
geneviewrs758927662
scholarrs758927662
googlers758927662
pharmgkbrs758927662
gwascentralrs758927662
openSNPrs758927662
23andMers758927662
23andMe allrs758927662
SNP Nexus

SNPshotrs758927662
SNPdbers758927662
MSV3drs758927662
GWAS Ctlgrs758927662
Max Magnitude0
ClinVar
Risk rs758927662(C,G;C,G)
Alt rs758927662(C,G;C,G)
Reference rs758927662(T;T)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11213374T>G
CLNSRC LDLR @ LOVD
CLNACC RCV000238146.1,