Have questions? Visit https://www.reddit.com/r/SNPedia

rs1823172

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1823172(A;A)
Make rs1823172(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position127308069
is asnp
is mentioned by
dbSNPrs1823172
ebirs1823172
HLIrs1823172
Exacrs1823172
Varsomers1823172
Maprs1823172
PheGenIrs1823172
hapmaprs1823172
1000 genomesrs1823172
hgdprs1823172
ensemblrs1823172
gopubmedrs1823172
geneviewrs1823172
scholarrs1823172
googlers1823172
pharmgkbrs1823172
gwascentralrs1823172
openSNPrs1823172
23andMers1823172
23andMe allrs1823172
SNP Nexus

SNPshotrs1823172
SNPdbers1823172
MSV3drs1823172
GWAS Ctlgrs1823172
GMAF0.2241
Max Magnitude0
? (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 5E-7
Odds Ratio 1.1700 [1.10-1.25]