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rs28931578

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28931578(A;A)
Make rs28931578(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44908751
GeneAPOE
is asnp
is mentioned by
dbSNPrs28931578
ebirs28931578
HLIrs28931578
Exacrs28931578
Varsomers28931578
Maprs28931578
PheGenIrs28931578
hapmaprs28931578
1000 genomesrs28931578
hgdprs28931578
ensemblrs28931578
gopubmedrs28931578
geneviewrs28931578
scholarrs28931578
googlers28931578
pharmgkbrs28931578
gwascentralrs28931578
openSNPrs28931578
23andMers28931578
23andMe allrs28931578
SNP Nexus

SNPshotrs28931578
SNPdbers28931578
MSV3drs28931578
GWAS Ctlgrs28931578
Max Magnitude0
OMIM107741
DescAPOE2 VARIANT
Variant0027
Relatedalso
Neighborrs429358
Distance67
Neighborrs769455
Distance32


ClinVar
Risk rs28931578(A,C;A,C)
Alt rs28931578(A,C;A,C)
Reference rs28931578(G;G)
Significance Pathogenic
Disease APOE2 VARIANT
Variation info
Gene APOE
CLNDBN APOE2 VARIANT
Reversed 0
HGVS NC_000019.9:g.45412008G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019460.28,