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rs16866933

From SNPedia

Orientationplus
Stabilizedplus
Make rs16866933(A;A)
Make rs16866933(A;G)
Make rs16866933(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position179701951
GeneZNF385B
is asnp
is mentioned by
dbSNPrs16866933
ebirs16866933
HLIrs16866933
Exacrs16866933
Varsomers16866933
Maprs16866933
PheGenIrs16866933
hapmaprs16866933
1000 genomesrs16866933
hgdprs16866933
ensemblrs16866933
gopubmedrs16866933
geneviewrs16866933
scholarrs16866933
googlers16866933
pharmgkbrs16866933
gwascentralrs16866933
openSNPrs16866933
23andMers16866933
23andMe allrs16866933
SNP Nexus

SNPshotrs16866933
SNPdbers16866933
MSV3drs16866933
GWAS Ctlgrs16866933
GMAF0.1492
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 6E-14
Odds Ratio 1.6900 [1.48-1.93]