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rs11710077

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs11710077(A;T)
Make rs11710077(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position38616408
GeneSCN5A
is asnp
is mentioned by
dbSNPrs11710077
ebirs11710077
HLIrs11710077
Exacrs11710077
Varsomers11710077
Maprs11710077
PheGenIrs11710077
hapmaprs11710077
1000 genomesrs11710077
hgdprs11710077
ensemblrs11710077
gopubmedrs11710077
geneviewrs11710077
scholarrs11710077
googlers11710077
pharmgkbrs11710077
gwascentralrs11710077
openSNPrs11710077
23andMers11710077
23andMe allrs11710077
SNP Nexus

SNPshotrs11710077
SNPdbers11710077
MSV3drs11710077
GWAS Ctlgrs11710077
GMAF0.1313
Max Magnitude0
? (A;A) (A;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 T
P-val 0.000001
Odds Ratio 0.4400 [NR] ms decrease