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rs9862154

From SNPedia

Orientationplus
Stabilizedplus
Make rs9862154(C;C)
Make rs9862154(C;G)
Make rs9862154(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position32080210
is asnp
is mentioned by
dbSNPrs9862154
ebirs9862154
HLIrs9862154
Exacrs9862154
Varsomers9862154
Maprs9862154
PheGenIrs9862154
hapmaprs9862154
1000 genomesrs9862154
hgdprs9862154
ensemblrs9862154
gopubmedrs9862154
geneviewrs9862154
scholarrs9862154
googlers9862154
pharmgkbrs9862154
gwascentralrs9862154
openSNPrs9862154
23andMers9862154
23andMe allrs9862154
SNP Nexus

SNPshotrs9862154
SNPdbers9862154
MSV3drs9862154
GWAS Ctlgrs9862154
GMAF0.3315
Max Magnitude
? (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