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rs121918381

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918381(A;G)
Make rs121918381(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position116832864
GeneAPOC3
is asnp
is mentioned by
dbSNPrs121918381
ebirs121918381
HLIrs121918381
Exacrs121918381
Varsomers121918381
Maprs121918381
PheGenIrs121918381
hapmaprs121918381
1000 genomesrs121918381
hgdprs121918381
ensemblrs121918381
gopubmedrs121918381
geneviewrs121918381
scholarrs121918381
googlers121918381
pharmgkbrs121918381
gwascentralrs121918381
openSNPrs121918381
23andMers121918381
23andMe allrs121918381
SNP Nexus

SNPshotrs121918381
SNPdbers121918381
MSV3drs121918381
GWAS Ctlgrs121918381
Max Magnitude0
OMIM107720
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918381(G;G)
Alt rs121918381(G;G)
Reference rs121918381(A;A)
Significance Pathogenic
Disease Apolipoprotein c-iii
Variation info
Gene APOC3
CLNDBN Apolipoprotein c-iii, nonglycosylated
Reversed 0
HGVS NC_000011.9:g.116703580A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019491.27,