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

rs1362212

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs1362212(A;A)
Make rs1362212(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position35265695
is asnp
is mentioned by
dbSNPrs1362212
ebirs1362212
HLIrs1362212
Exacrs1362212
Varsomers1362212
Maprs1362212
PheGenIrs1362212
hapmaprs1362212
1000 genomesrs1362212
hgdprs1362212
ensemblrs1362212
gopubmedrs1362212
geneviewrs1362212
scholarrs1362212
googlers1362212
pharmgkbrs1362212
gwascentralrs1362212
openSNPrs1362212
23andMers1362212
23andMe allrs1362212
SNP Nexus

SNPshotrs1362212
SNPdbers1362212
MSV3drs1362212
GWAS Ctlgrs1362212
GMAF0.09871
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21076409OA-icon.png]
Trait
Title Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Risk Allele A
P-val 1E-13
Odds Ratio 0.6900 [0.51-0.87] ms increase