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rs28931579

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs28931579(A;C)
Make rs28931579(C;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position44909236
GeneAPOE
is asnp
is mentioned by
dbSNPrs28931579
ebirs28931579
HLIrs28931579
Exacrs28931579
Varsomers28931579
Maprs28931579
PheGenIrs28931579
hapmaprs28931579
1000 genomesrs28931579
hgdprs28931579
ensemblrs28931579
gopubmedrs28931579
geneviewrs28931579
scholarrs28931579
googlers28931579
pharmgkbrs28931579
gwascentralrs28931579
openSNPrs28931579
23andMers28931579
23andMe allrs28931579
SNP Nexus

SNPshotrs28931579
SNPdbers28931579
MSV3drs28931579
GWAS Ctlgrs28931579
Max Magnitude0
OMIM107741
DescAPOE4(+)
Variant0029
Relatedalso
Neighborrs7412
Distance414


ClinVar
Risk rs28931579(C;C)
Alt rs28931579(C;C)
Reference rs28931579(A;A)
Significance Pathogenic
Disease APOE4(+)
Variation info
Gene APOE
CLNDBN APOE4(+)
Reversed 0
HGVS NC_000019.9:g.45412493A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019462.28,