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rs769383881

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs769383881(G;T)
Make rs769383881(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11105243
GeneLDLR
is asnp
is mentioned by
dbSNPrs769383881
ebirs769383881
HLIrs769383881
Exacrs769383881
Varsomers769383881
Maprs769383881
PheGenIrs769383881
hapmaprs769383881
1000 genomesrs769383881
hgdprs769383881
ensemblrs769383881
gopubmedrs769383881
geneviewrs769383881
scholarrs769383881
googlers769383881
pharmgkbrs769383881
gwascentralrs769383881
openSNPrs769383881
23andMers769383881
23andMe allrs769383881
SNP Nexus

SNPshotrs769383881
SNPdbers769383881
MSV3drs769383881
GWAS Ctlgrs769383881
Max Magnitude0
ClinVar
Risk rs769383881(A,T;A,T)
Alt rs769383881(A,T;A,T)
Reference rs769383881(G;G)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11215919G>A; NC_000019.9:g.11215919G>T
CLNSRC LDLR @ LOVD
CLNACC RCV000232879.2, RCV000211560.2,