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rs121918382

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918382(A;G)
Make rs121918382(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position116832816
GeneAPOC3
is asnp
is mentioned by
dbSNPrs121918382
ebirs121918382
HLIrs121918382
Exacrs121918382
Varsomers121918382
Maprs121918382
PheGenIrs121918382
hapmaprs121918382
1000 genomesrs121918382
hgdprs121918382
ensemblrs121918382
gopubmedrs121918382
geneviewrs121918382
scholarrs121918382
googlers121918382
pharmgkbrs121918382
gwascentralrs121918382
openSNPrs121918382
23andMers121918382
23andMe allrs121918382
SNP Nexus

SNPshotrs121918382
SNPdbers121918382
MSV3drs121918382
GWAS Ctlgrs121918382
Max Magnitude0
OMIM107720
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121918382(G;G)
Alt rs121918382(G;G)
Reference rs121918382(A;A)
Significance Pathogenic
Disease Hyperalphalipoproteinemia 2
Variation info
Gene APOC3
CLNDBN Hyperalphalipoproteinemia 2
Reversed 0
HGVS NC_000011.9:g.116703532A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019492.24,