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rs783396

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs783396(A;A)
Make rs783396(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position106539495
GeneAIM1
is asnp
is mentioned by
dbSNPrs783396
ebirs783396
HLIrs783396
Exacrs783396
Varsomers783396
Maprs783396
PheGenIrs783396
hapmaprs783396
1000 genomesrs783396
hgdprs783396
ensemblrs783396
gopubmedrs783396
geneviewrs783396
scholarrs783396
googlers783396
pharmgkbrs783396
gwascentralrs783396
openSNPrs783396
23andMers783396
23andMe allrs783396
SNP Nexus

SNPshotrs783396
SNPdbers783396
MSV3drs783396
GWAS Ctlgrs783396
GMAF0.07208
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS
SNP rs783396
PubMedID [PMID 17434096OA-icon.png]
Condition Stroke
Gene AIM1
Risk Allele
pValue 9.00E-006
OR 2.17
95% CI 1.47-3.13



[PMID 22403240OA-icon.png] Associations Between Incident Ischemic Stroke Events and Stroke and Cardiovascular Disease-Related GWAS SNPs in the Population Architecture Using Genomics and Epidemiology (PAGE) Study


GET Evidence
AIM1-E1196A
aa_change Glu1196Ala
aa_change_short E1196A
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.929727
summary