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rs17450029

From SNPedia

Orientationplus
Stabilizedplus
Make rs17450029(C;C)
Make rs17450029(C;T)
Make rs17450029(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position101075443
GeneLOC102606465
is asnp
is mentioned by
dbSNPrs17450029
dbSNP (classic)rs17450029
ClinGenrs17450029
ebirs17450029
HLIrs17450029
Exacrs17450029
Gnomadrs17450029
Varsomers17450029
LitVarrs17450029
Maprs17450029
PheGenIrs17450029
Biobankrs17450029
1000 genomesrs17450029
hgdprs17450029
ensemblrs17450029
geneviewrs17450029
scholarrs17450029
googlers17450029
pharmgkbrs17450029
gwascentralrs17450029
openSNPrs17450029
23andMers17450029
SNPshotrs17450029
SNPdbers17450029
MSV3drs17450029
GWAS Ctlgrs17450029
GMAF0.197
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23459443OA-icon.png]
Trait QT interval (interaction)
Title Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.
Risk Allele T
P-val 3E-6
Odds Ratio NR NR