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rs4687718

From SNPedia

Orientationplus
Stabilizedplus
Make rs4687718(A;A)
Make rs4687718(A;G)
Make rs4687718(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position53248287
GeneTKT
is asnp
is mentioned by
dbSNPrs4687718
ebirs4687718
HLIrs4687718
Exacrs4687718
Varsomers4687718
Maprs4687718
PheGenIrs4687718
hapmaprs4687718
1000 genomesrs4687718
hgdprs4687718
ensemblrs4687718
gopubmedrs4687718
geneviewrs4687718
scholarrs4687718
googlers4687718
pharmgkbrs4687718
gwascentralrs4687718
openSNPrs4687718
23andMers4687718
23andMe allrs4687718
SNP Nexus

SNPshotrs4687718
SNPdbers4687718
MSV3drs4687718
GWAS Ctlgrs4687718
GMAF0.2048
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 6E-9
Odds Ratio 0.6300 [0.41-0.85] ms decrease