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rs7784776

From SNPedia

Orientationplus
Stabilizedplus
Make rs7784776(A;A)
Make rs7784776(A;G)
Make rs7784776(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position46580547
is asnp
is mentioned by
dbSNPrs7784776
ebirs7784776
HLIrs7784776
Exacrs7784776
Varsomers7784776
Maprs7784776
PheGenIrs7784776
hapmaprs7784776
1000 genomesrs7784776
hgdprs7784776
ensemblrs7784776
gopubmedrs7784776
geneviewrs7784776
scholarrs7784776
googlers7784776
pharmgkbrs7784776
gwascentralrs7784776
openSNPrs7784776
23andMers7784776
23andMe allrs7784776
SNP Nexus

SNPshotrs7784776
SNPdbers7784776
MSV3drs7784776
GWAS Ctlgrs7784776
GMAF0.4844
Max Magnitude
? (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 G
P-val 1E-9
Odds Ratio 0.3900 [0.25-0.53] ms increase