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rs767024374

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs767024374(C;T)
Make rs767024374(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11110719
GeneLDLR
is asnp
is mentioned by
dbSNPrs767024374
ebirs767024374
HLIrs767024374
Exacrs767024374
Varsomers767024374
Maprs767024374
PheGenIrs767024374
hapmaprs767024374
1000 genomesrs767024374
hgdprs767024374
ensemblrs767024374
gopubmedrs767024374
geneviewrs767024374
scholarrs767024374
googlers767024374
pharmgkbrs767024374
gwascentralrs767024374
openSNPrs767024374
23andMers767024374
23andMe allrs767024374
SNP Nexus

SNPshotrs767024374
SNPdbers767024374
MSV3drs767024374
GWAS Ctlgrs767024374
Max Magnitude0
ClinVar
Risk rs767024374(T;T)
Alt rs767024374(T;T)
Reference rs767024374(C;C)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11221395C>A
CLNSRC LDLR @ LOVD
CLNACC RCV000238137.1,