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rs766094434

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs766094434(A;A)
Make rs766094434(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11105371
GeneLDLR
is asnp
is mentioned by
dbSNPrs766094434
ebirs766094434
HLIrs766094434
Exacrs766094434
Varsomers766094434
Maprs766094434
PheGenIrs766094434
hapmaprs766094434
1000 genomesrs766094434
hgdprs766094434
ensemblrs766094434
gopubmedrs766094434
geneviewrs766094434
scholarrs766094434
googlers766094434
pharmgkbrs766094434
gwascentralrs766094434
openSNPrs766094434
23andMers766094434
23andMe allrs766094434
SNP Nexus

SNPshotrs766094434
SNPdbers766094434
MSV3drs766094434
GWAS Ctlgrs766094434
Max Magnitude0
ClinVar
Risk rs766094434(A;A)
Alt rs766094434(A;A)
Reference rs766094434(C;C)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11216047C>A
CLNSRC LDLR @ LOVD
CLNACC RCV000237702.1,