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

rs121909576

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909576(A;A)
Make rs121909576(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position116821310
GeneAPOA4
is asnp
is mentioned by
dbSNPrs121909576
ebirs121909576
HLIrs121909576
Exacrs121909576
Varsomers121909576
Maprs121909576
PheGenIrs121909576
hapmaprs121909576
1000 genomesrs121909576
hgdprs121909576
ensemblrs121909576
gopubmedrs121909576
geneviewrs121909576
scholarrs121909576
googlers121909576
pharmgkbrs121909576
gwascentralrs121909576
openSNPrs121909576
23andMers121909576
23andMe allrs121909576
SNP Nexus

SNPshotrs121909576
SNPdbers121909576
MSV3drs121909576
GWAS Ctlgrs121909576
Max Magnitude0
OMIM107690
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909576(A;A)
Alt rs121909576(A;A)
Reference rs121909576(G;G)
Significance Other
Disease APOLIPOPROTEIN A-IV RARE VARIANT
Variation info
Gene APOA4
CLNDBN APOLIPOPROTEIN A-IV RARE VARIANT, APOA4*3
Reversed 1
HGVS NC_000011.9:g.116692026C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019496.24,