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rs777640882

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs777640882(C;G)
Make rs777640882(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11102740
GeneLDLR
is asnp
is mentioned by
dbSNPrs777640882
ebirs777640882
HLIrs777640882
Exacrs777640882
Varsomers777640882
Maprs777640882
PheGenIrs777640882
hapmaprs777640882
1000 genomesrs777640882
hgdprs777640882
ensemblrs777640882
gopubmedrs777640882
geneviewrs777640882
scholarrs777640882
googlers777640882
pharmgkbrs777640882
gwascentralrs777640882
openSNPrs777640882
23andMers777640882
23andMe allrs777640882
SNP Nexus

SNPshotrs777640882
SNPdbers777640882
MSV3drs777640882
GWAS Ctlgrs777640882
Max Magnitude0
ClinVar
Risk rs777640882(G,T;G,T)
Alt rs777640882(G,T;G,T)
Reference rs777640882(C;C)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11213416C>G
CLNSRC LDLR @ LOVD
CLNACC RCV000237969.1,