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rs991014

From SNPedia

Orientationminus
Stabilizedminus
Make rs991014(A;A)
Make rs991014(A;G)
Make rs991014(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position44859921
GeneSETBP1
is asnp
is mentioned by
dbSNPrs991014
ebirs991014
HLIrs991014
Exacrs991014
Varsomers991014
Maprs991014
PheGenIrs991014
hapmaprs991014
1000 genomesrs991014
hgdprs991014
ensemblrs991014
gopubmedrs991014
geneviewrs991014
scholarrs991014
googlers991014
pharmgkbrs991014
gwascentralrs991014
openSNPrs991014
23andMers991014
23andMe allrs991014
SNP Nexus

SNPshotrs991014
SNPdbers991014
MSV3drs991014
GWAS Ctlgrs991014
GMAF0.3297
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 T
P-val 6E-10
Odds Ratio 0.4200 [0.28-0.56] ms increase