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rs767790696

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs767790696(A;G)
Make rs767790696(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11129511
GeneLDLR
is asnp
is mentioned by
dbSNPrs767790696
ebirs767790696
HLIrs767790696
Exacrs767790696
Varsomers767790696
Maprs767790696
PheGenIrs767790696
hapmaprs767790696
1000 genomesrs767790696
hgdprs767790696
ensemblrs767790696
gopubmedrs767790696
geneviewrs767790696
scholarrs767790696
googlers767790696
pharmgkbrs767790696
gwascentralrs767790696
openSNPrs767790696
23andMers767790696
23andMe allrs767790696
SNP Nexus

SNPshotrs767790696
SNPdbers767790696
MSV3drs767790696
GWAS Ctlgrs767790696
Max Magnitude0
ClinVar
Risk rs767790696(G;G)
Alt rs767790696(G;G)
Reference rs767790696(A;A)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11240187A>G
CLNSRC LDLR @ LOVD
CLNACC RCV000238115.1,