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rs11708189

From SNPedia

Orientationplus
Stabilizedplus
Make rs11708189(A;A)
Make rs11708189(A;G)
Make rs11708189(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position140456518
GeneCLSTN2
is asnp
is mentioned by
dbSNPrs11708189
ebirs11708189
HLIrs11708189
Exacrs11708189
Varsomers11708189
Maprs11708189
PheGenIrs11708189
hapmaprs11708189
1000 genomesrs11708189
hgdprs11708189
ensemblrs11708189
gopubmedrs11708189
geneviewrs11708189
scholarrs11708189
googlers11708189
pharmgkbrs11708189
gwascentralrs11708189
openSNPrs11708189
23andMers11708189
23andMe allrs11708189
SNP Nexus

SNPshotrs11708189
SNPdbers11708189
MSV3drs11708189
GWAS Ctlgrs11708189
GMAF0.4651
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21658281OA-icon.png]
Trait
Title GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.
Risk Allele
P-val 0.000002
Odds Ratio 1.1200 [1.07-1.18]