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rs121918396

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918396(A;A)
Make rs121918396(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44908979
GeneAPOE
is asnp
is mentioned by
dbSNPrs121918396
ebirs121918396
HLIrs121918396
Exacrs121918396
Varsomers121918396
Maprs121918396
PheGenIrs121918396
hapmaprs121918396
1000 genomesrs121918396
hgdprs121918396
ensemblrs121918396
gopubmedrs121918396
geneviewrs121918396
scholarrs121918396
googlers121918396
pharmgkbrs121918396
gwascentralrs121918396
openSNPrs121918396
23andMers121918396
23andMe allrs121918396
SNP Nexus

SNPshotrs121918396
SNPdbers121918396
MSV3drs121918396
GWAS Ctlgrs121918396
Max Magnitude0
OMIM107741
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121918396(A;A)
Alt rs121918396(A;A)
Reference rs121918396(G;G)
Significance Pathogenic
Disease Familial type 3 hyperlipoproteinemia APOE3-WASHINGTON
Variation info
Gene APOE
CLNDBN Familial type 3 hyperlipoproteinemia APOE3-WASHINGTON
Reversed 0
HGVS NC_000019.9:g.45412236G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019445.23, RCV000019446.23,