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rs7562790

From SNPedia

Orientationplus
Stabilizedplus
Make rs7562790(G;G)
Make rs7562790(G;T)
Make rs7562790(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position36446412
GeneCRIM1
is asnp
is mentioned by
dbSNPrs7562790
ebirs7562790
HLIrs7562790
Exacrs7562790
Varsomers7562790
Maprs7562790
PheGenIrs7562790
hapmaprs7562790
1000 genomesrs7562790
hgdprs7562790
ensemblrs7562790
gopubmedrs7562790
geneviewrs7562790
scholarrs7562790
googlers7562790
pharmgkbrs7562790
gwascentralrs7562790
openSNPrs7562790
23andMers7562790
23andMe allrs7562790
SNP Nexus

SNPshotrs7562790
SNPdbers7562790
MSV3drs7562790
GWAS Ctlgrs7562790
GMAF0.472
Max Magnitude
? (G;G) (G;T) (T;T) 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 G
P-val 8E-9
Odds Ratio 0.3900 [0.25-0.53] ms increase