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rs9851724

From SNPedia

Orientationplus
Stabilizedplus
Make rs9851724(C;C)
Make rs9851724(C;T)
Make rs9851724(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position38678444
is asnp
is mentioned by
dbSNPrs9851724
ebirs9851724
HLIrs9851724
Exacrs9851724
Varsomers9851724
Maprs9851724
PheGenIrs9851724
hapmaprs9851724
1000 genomesrs9851724
hgdprs9851724
ensemblrs9851724
gopubmedrs9851724
geneviewrs9851724
scholarrs9851724
googlers9851724
pharmgkbrs9851724
gwascentralrs9851724
openSNPrs9851724
23andMers9851724
23andMe allrs9851724
SNP Nexus

SNPshotrs9851724
SNPdbers9851724
MSV3drs9851724
GWAS Ctlgrs9851724
GMAF0.2732
Max Magnitude
? (C;C) (C;T) (T;T) 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 C
P-val 6E-16
Odds Ratio 0.6000 [NR] ms decrease