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rs2074238

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs2074238(C;T)
Make rs2074238(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2463573
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs2074238
ebirs2074238
HLIrs2074238
Exacrs2074238
Varsomers2074238
Maprs2074238
PheGenIrs2074238
hapmaprs2074238
1000 genomesrs2074238
hgdprs2074238
ensemblrs2074238
gopubmedrs2074238
geneviewrs2074238
scholarrs2074238
googlers2074238
pharmgkbrs2074238
gwascentralrs2074238
openSNPrs2074238
23andMers2074238
23andMe allrs2074238
SNP Nexus

SNPshotrs2074238
SNPdbers2074238
MSV3drs2074238
GWAS Ctlgrs2074238
GMAF0.04178
Max Magnitude0
? (C;C) (C;T) (T;T) 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 T
P-val 3E-17
Odds Ratio 7.88 [6.16-9.59] msec decrease



GET Evidence
rs2074238
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.951613
summary



[PMID 23856471OA-icon.png] Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome.