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rs37062

From SNPedia

Orientationplus
Stabilizedplus
Make rs37062(A;A)
Make rs37062(A;G)
Make rs37062(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position58533334
GeneCNOT1
is asnp
is mentioned by
dbSNPrs37062
ebirs37062
HLIrs37062
Exacrs37062
Varsomers37062
Maprs37062
PheGenIrs37062
hapmaprs37062
1000 genomesrs37062
hgdprs37062
ensemblrs37062
gopubmedrs37062
geneviewrs37062
scholarrs37062
googlers37062
pharmgkbrs37062
gwascentralrs37062
openSNPrs37062
23andMers37062
23andMe allrs37062
SNP Nexus

SNPshotrs37062
SNPdbers37062
MSV3drs37062
GWAS Ctlgrs37062
GMAF0.2837
Max Magnitude
? (A;A) (A;G) (G;G) 28
23andMe blog Influences QT interval
GWAS snp
PMID [PMID 19305408OA-icon.png]
Trait QT interval
Title Common variants at ten loci influence QT interval duation in the QTGEN Study
Risk Allele G
P-val 3E-25
Odds Ratio 1.75 [1.41-2.09] msec decrease


GWAS snp
PMID [PMID 20062063]
Trait Electrocardiographic traits
Title Several common variants modulate heart rate, PR interval and QRS duration
Risk Allele A
P-val 0.000001
Odds Ratio 6.09 [3.62-8.57] % SD increase


GET Evidence
rs37062
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.277778
summary