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rs121918398

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918398(A;A)
Make rs121918398(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44909171
GeneAPOE
is asnp
is mentioned by
dbSNPrs121918398
ebirs121918398
HLIrs121918398
Exacrs121918398
Varsomers121918398
Maprs121918398
PheGenIrs121918398
hapmaprs121918398
1000 genomesrs121918398
hgdprs121918398
ensemblrs121918398
gopubmedrs121918398
geneviewrs121918398
scholarrs121918398
googlers121918398
pharmgkbrs121918398
gwascentralrs121918398
openSNPrs121918398
23andMers121918398
23andMe allrs121918398
SNP Nexus

SNPshotrs121918398
SNPdbers121918398
MSV3drs121918398
GWAS Ctlgrs121918398
Max Magnitude0
OMIM107741
Desc
Variant0028
Relatedalso
ClinVar
Risk rs121918398(A;A)
Alt rs121918398(A;A)
Reference rs121918398(G;G)
Significance Pathogenic
Disease APOE4 VARIANT
Variation info
Gene APOE
CLNDBN APOE4 VARIANT
Reversed 0
HGVS NC_000019.9:g.45412428G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019461.28,