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rs28931576

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs28931576(A;G)
Make rs28931576(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44907894
GeneAPOE
is asnp
is mentioned by
dbSNPrs28931576
ebirs28931576
HLIrs28931576
Exacrs28931576
Varsomers28931576
Maprs28931576
PheGenIrs28931576
hapmaprs28931576
1000 genomesrs28931576
hgdprs28931576
ensemblrs28931576
gopubmedrs28931576
geneviewrs28931576
scholarrs28931576
googlers28931576
pharmgkbrs28931576
gwascentralrs28931576
openSNPrs28931576
23andMers28931576
23andMe allrs28931576
SNP Nexus

SNPshotrs28931576
SNPdbers28931576
MSV3drs28931576
GWAS Ctlgrs28931576
Max Magnitude0
OMIM107741
DescAPOE3(-)-FREIBURG
Variant0024
Relatedalso

The ancestral allele is A.

Neighborrs769452
Distance41
Neighborrs11083750
Distance707


ClinVar
Risk rs28931576(G;G)
Alt rs28931576(G;G)
Reference rs28931576(A;A)
Significance Pathogenic
Disease APOE3(-)-FREIBURG
Variation info
Gene APOE
CLNDBN APOE3(-)-FREIBURG
Reversed 0
HGVS NC_000019.9:g.45411151A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019457.23,