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rs11153730

From SNPedia

Orientationplus
Stabilizedplus
Make rs11153730(C;C)
Make rs11153730(C;T)
Make rs11153730(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position118346359
is asnp
is mentioned by
dbSNPrs11153730
dbSNP (classic)rs11153730
ClinGenrs11153730
ebirs11153730
HLIrs11153730
Exacrs11153730
Gnomadrs11153730
Varsomers11153730
LitVarrs11153730
Maprs11153730
PheGenIrs11153730
Biobankrs11153730
1000 genomesrs11153730
hgdprs11153730
ensemblrs11153730
geneviewrs11153730
scholarrs11153730
googlers11153730
pharmgkbrs11153730
gwascentralrs11153730
openSNPrs11153730
23andMers11153730
SNPshotrs11153730
SNPdbers11153730
MSV3drs11153730
GWAS Ctlgrs11153730
GMAF0.3388
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 19587794OA-icon.png] Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies

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 C
P-val 1E-18
Odds Ratio 0.5900 [0.45-0.73] ms increase
GWAS snp
PMID [PMID 23583979OA-icon.png]
Trait Heart rate
Title Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.
Risk Allele T
P-val 8E-21
Odds Ratio .38 [0.29-0.47] unit increase