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rs7188697

From SNPedia

Orientationplus
Stabilizedplus
Make rs7188697(A;A)
Make rs7188697(A;G)
Make rs7188697(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position58588274
GeneCNOT1
is asnp
is mentioned by
dbSNPrs7188697
ebirs7188697
HLIrs7188697
Exacrs7188697
Varsomers7188697
Maprs7188697
PheGenIrs7188697
hapmaprs7188697
1000 genomesrs7188697
hgdprs7188697
ensemblrs7188697
gopubmedrs7188697
geneviewrs7188697
scholarrs7188697
googlers7188697
pharmgkbrs7188697
gwascentralrs7188697
openSNPrs7188697
23andMers7188697
23andMe allrs7188697
SNP Nexus

SNPshotrs7188697
SNPdbers7188697
MSV3drs7188697
GWAS Ctlgrs7188697
GMAF0.2897
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19305409OA-icon.png]
Trait QT interval
Title Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Risk Allele A
P-val 7E-25
Odds Ratio 1.66 [1.20-2.12] ms increase



GET Evidence
rs7188697
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.710938
summary