Have questions? Visit https://www.reddit.com/r/SNPedia

rs12296050

From SNPedia

Orientationplus
Stabilizedplus
Make rs12296050(C;C)
Make rs12296050(C;T)
Make rs12296050(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2468112
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs12296050
ebirs12296050
HLIrs12296050
Exacrs12296050
Varsomers12296050
Maprs12296050
PheGenIrs12296050
hapmaprs12296050
1000 genomesrs12296050
hgdprs12296050
ensemblrs12296050
gopubmedrs12296050
geneviewrs12296050
scholarrs12296050
googlers12296050
pharmgkbrs12296050
gwascentralrs12296050
openSNPrs12296050
23andMers12296050
23andMe allrs12296050
SNP Nexus

SNPshotrs12296050
SNPdbers12296050
MSV3drs12296050
GWAS Ctlgrs12296050
GMAF0.371
Max Magnitude
? (C;C) (C;T) (T;T) 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 T
P-val 3E-17
Odds Ratio 1.44 [0.95-1.93] ms increase


GWAS snp
PMID [PMID 20062063]
Trait Electrocardiographic traits
Title Several common variants modulate heart rate, PR interval and QRS duration
Risk Allele T
P-val 8E-11
Odds Ratio 13.16 [9.19-17.12] % SD increase


GET Evidence
rs12296050
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.40625
summary



[PMID 23692438] Association between KCNQ1 genetic variants and QT interval in a Chinese population.