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rs1733724

From SNPedia

Orientationminus
Stabilizedminus
Make rs1733724(C;C)
Make rs1733724(C;T)
Make rs1733724(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position52464217
GeneLINC01468
is asnp
is mentioned by
dbSNPrs1733724
ebirs1733724
HLIrs1733724
Exacrs1733724
Varsomers1733724
Maprs1733724
PheGenIrs1733724
hapmaprs1733724
1000 genomesrs1733724
hgdprs1733724
ensemblrs1733724
gopubmedrs1733724
geneviewrs1733724
scholarrs1733724
googlers1733724
pharmgkbrs1733724
gwascentralrs1733724
openSNPrs1733724
23andMers1733724
23andMe allrs1733724
SNP Nexus

SNPshotrs1733724
SNPdbers1733724
MSV3drs1733724
GWAS Ctlgrs1733724
GMAF0.141
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20062063]
Trait Electrocardiographic traits
Title Several common variants modulate heart rate, PR interval and QRS duration
Risk Allele T
P-val 7E-8
Odds Ratio 5.62 [3.58-7.66] % SD increase
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 3E-8
Odds Ratio 0.4900 [0.31-0.67] ms increase