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rs13165478

From SNPedia

Orientationplus
Stabilizedplus
Make rs13165478(A;A)
Make rs13165478(A;G)
Make rs13165478(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position154489480
is asnp
is mentioned by
dbSNPrs13165478
ebirs13165478
HLIrs13165478
Exacrs13165478
Varsomers13165478
Maprs13165478
PheGenIrs13165478
hapmaprs13165478
1000 genomesrs13165478
hgdprs13165478
ensemblrs13165478
gopubmedrs13165478
geneviewrs13165478
scholarrs13165478
googlers13165478
pharmgkbrs13165478
gwascentralrs13165478
openSNPrs13165478
23andMers13165478
23andMe allrs13165478
SNP Nexus

SNPshotrs13165478
SNPdbers13165478
MSV3drs13165478
GWAS Ctlgrs13165478
GMAF0.3994
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 A
P-val 7E-14
Odds Ratio 0.5500 [0.41-0.69] ms decrease