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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
ebirs11153730
HLIrs11153730
Exacrs11153730
Varsomers11153730
Maprs11153730
PheGenIrs11153730
hapmaprs11153730
1000 genomesrs11153730
hgdprs11153730
ensemblrs11153730
gopubmedrs11153730
geneviewrs11153730
scholarrs11153730
googlers11153730
pharmgkbrs11153730
gwascentralrs11153730
openSNPrs11153730
23andMers11153730
23andMe allrs11153730
SNP Nexus

SNPshotrs11153730
SNPdbers11153730
MSV3drs11153730
GWAS Ctlgrs11153730
GMAF0.3388
Max Magnitude
? (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
GET Evidence
rs11153730
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.390625
summary


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