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rs17779747

From SNPedia

Orientationplus
Stabilizedplus
Make rs17779747(G;G)
Make rs17779747(G;T)
Make rs17779747(T;T)
ReferenceGRCh37 37.1/131
Chromosome17
Position68494992
is asnp
is mentioned by
dbSNPrs17779747
ebirs17779747
HLIrs17779747
Exacrs17779747
Varsomers17779747
Maprs17779747
PheGenIrs17779747
hapmaprs17779747
1000 genomesrs17779747
hgdprs17779747
ensemblrs17779747
gopubmedrs17779747
geneviewrs17779747
scholarrs17779747
googlers17779747
pharmgkbrs17779747
gwascentralrs17779747
openSNPrs17779747
23andMers17779747
23andMe allrs17779747
SNP Nexus

SNPshotrs17779747
SNPdbers17779747
MSV3drs17779747
GWAS Ctlgrs17779747
GMAF0.1974
Max Magnitude
? (G;G) (G;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 6E-12
Odds Ratio 1.02 [0.53-1.51] ms decrease


[PMID 19305408OA-icon.png] Common variants at ten loci influence QT interval duration in the QTGEN Study.


GET Evidence
rs17779747
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.203125
summary



[PMID 25819866] Genetic markers of repolarization and arrhythmic events after acute coronary syndromes