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rs773328511

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773328511(A;A)
Make rs773328511(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11106680
GeneLDLR
is asnp
is mentioned by
dbSNPrs773328511
ebirs773328511
HLIrs773328511
Exacrs773328511
Varsomers773328511
Maprs773328511
PheGenIrs773328511
hapmaprs773328511
1000 genomesrs773328511
hgdprs773328511
ensemblrs773328511
gopubmedrs773328511
geneviewrs773328511
scholarrs773328511
googlers773328511
pharmgkbrs773328511
gwascentralrs773328511
openSNPrs773328511
23andMers773328511
23andMe allrs773328511
SNP Nexus

SNPshotrs773328511
SNPdbers773328511
MSV3drs773328511
GWAS Ctlgrs773328511
Max Magnitude0
ClinVar
Risk rs773328511(A,T;A,T)
Alt rs773328511(A,T;A,T)
Reference rs773328511(C;C)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11217356C>A; NC_000019.9:g.11217356C>T
CLNSRC LDLR @ LOVD
CLNACC RCV000238441.1, RCV000237636.1,