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rs7781293

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;C) 0 common in complete genomics
Make rs7781293(A;A)
Make rs7781293(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position15451358
GeneAGMO
is asnp
is mentioned by
dbSNPrs7781293
ebirs7781293
HLIrs7781293
Exacrs7781293
Varsomers7781293
Maprs7781293
PheGenIrs7781293
hapmaprs7781293
1000 genomesrs7781293
hgdprs7781293
ensemblrs7781293
gopubmedrs7781293
geneviewrs7781293
scholarrs7781293
googlers7781293
pharmgkbrs7781293
gwascentralrs7781293
openSNPrs7781293
23andMers7781293
23andMe allrs7781293
SNP Nexus

SNPshotrs7781293
SNPdbers7781293
MSV3drs7781293
GWAS Ctlgrs7781293
GMAF0.4605
Max Magnitude0
? (A;A) (A;C) (C;C) 28

[PMID 20613766] Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms