Have questions? Visit https://www.reddit.com/r/SNPedia

rs121917821

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917821(C;T)
Make rs121917821(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116790814
GeneAPOA5
is asnp
is mentioned by
dbSNPrs121917821
ebirs121917821
HLIrs121917821
Exacrs121917821
Varsomers121917821
Maprs121917821
PheGenIrs121917821
hapmaprs121917821
1000 genomesrs121917821
hgdprs121917821
ensemblrs121917821
gopubmedrs121917821
geneviewrs121917821
scholarrs121917821
googlers121917821
pharmgkbrs121917821
gwascentralrs121917821
openSNPrs121917821
23andMers121917821
23andMe allrs121917821
SNP Nexus

SNPshotrs121917821
SNPdbers121917821
MSV3drs121917821
GWAS Ctlgrs121917821
Max Magnitude0
ClinVar
Risk rs121917821(T;T)
Alt rs121917821(T;T)
Reference rs121917821(C;C)
Significance Pathogenic
Disease Familial type 5 hyperlipoproteinemia
Variation info
Gene APOA5
CLNDBN Familial type 5 hyperlipoproteinemia
Reversed 1
HGVS NC_000011.9:g.116661530G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004654.3,