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rs769452

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs769452(C;C)
Make rs769452(C;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position44907853
GeneAPOE
is asnp
is mentioned by
dbSNPrs769452
ClinGenrs769452
ebirs769452
HLIrs769452
Exacrs769452
Varsomers769452
Maprs769452
PheGenIrs769452
hapmaprs769452
1000 genomesrs769452
hgdprs769452
ensemblrs769452
gopubmedrs769452
geneviewrs769452
scholarrs769452
googlers769452
pharmgkbrs769452
gwascentralrs769452
openSNPrs769452
23andMers769452
23andMe allrs769452
SNP Nexus

SNPshotrs769452
SNPdbers769452
MSV3drs769452
GWAS Ctlgrs769452
GMAF0.001377
Max Magnitude0
OMIM107741
DescAPOE4(-)-FREIBURG
Variant0023
Relatedalso
Neighborrs28931576
Distance41


ClinVar
Risk rs769452(C;C)
Alt rs769452(C;C)
Reference Rs769452(T;T)
Significance Pathogenic
Disease APOE4(-)-FREIBURG not specified
Variation info
Gene APOE
CLNDBN APOE4(-)-FREIBURG not specified
Reversed 0
HGVS NC_000019.9:g.45411110T>C
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000019456.28, RCV000429606.1,



[PMID 17672902OA-icon.png] Subarachnoid hemorrhage: tests of association with apolipoprotein E and elastin genes.