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rs12084280

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs12084280(C;C)
Make rs12084280(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position162054019
is asnp
is mentioned by
dbSNPrs12084280
ebirs12084280
HLIrs12084280
Exacrs12084280
Varsomers12084280
Maprs12084280
PheGenIrs12084280
hapmaprs12084280
1000 genomesrs12084280
hgdprs12084280
ensemblrs12084280
gopubmedrs12084280
geneviewrs12084280
scholarrs12084280
googlers12084280
pharmgkbrs12084280
gwascentralrs12084280
openSNPrs12084280
23andMers12084280
23andMe allrs12084280
SNP Nexus

SNPshotrs12084280
SNPdbers12084280
MSV3drs12084280
GWAS Ctlgrs12084280
GMAF0.2544
Max Magnitude0
? (C;C) (C;G) (G;G) 28
[PMID 21685173OA-icon.png] Common Variants in CASQ2, GPD1L and NOS1AP Are Significantly Associated with Risk of Sudden Death in Patients with Coronary Artery Disease


[PMID 23171141OA-icon.png] Positive association between rs10918859 of the NOS1AP gene and coronary heart disease in male Han Chinese.