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rs121918395

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918395(C;T)
Make rs121918395(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position44909032
GeneAPOE
is asnp
is mentioned by
dbSNPrs121918395
ebirs121918395
HLIrs121918395
Exacrs121918395
Varsomers121918395
Maprs121918395
PheGenIrs121918395
hapmaprs121918395
1000 genomesrs121918395
hgdprs121918395
ensemblrs121918395
gopubmedrs121918395
geneviewrs121918395
scholarrs121918395
googlers121918395
pharmgkbrs121918395
gwascentralrs121918395
openSNPrs121918395
23andMers121918395
23andMe allrs121918395
SNP Nexus

SNPshotrs121918395
SNPdbers121918395
MSV3drs121918395
GWAS Ctlgrs121918395
Max Magnitude0
OMIM107741
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121918395(T;T)
Alt rs121918395(T;T)
Reference rs121918395(C;C)
Significance Pathogenic
Disease APOE2-DUNEDIN
Variation info
Gene APOE
CLNDBN APOE2-DUNEDIN
Reversed 0
HGVS NC_000019.9:g.45412289C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019442.24,