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rs9947295

From SNPedia

Orientationplus
Stabilizedplus
Make rs9947295(C;C)
Make rs9947295(C;T)
Make rs9947295(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position11759433
GeneGNAL
is asnp
is mentioned by
dbSNPrs9947295
ebirs9947295
HLIrs9947295
Exacrs9947295
Varsomers9947295
Maprs9947295
PheGenIrs9947295
hapmaprs9947295
1000 genomesrs9947295
hgdprs9947295
ensemblrs9947295
gopubmedrs9947295
geneviewrs9947295
scholarrs9947295
googlers9947295
pharmgkbrs9947295
gwascentralrs9947295
openSNPrs9947295
23andMers9947295
23andMe allrs9947295
SNP Nexus

SNPshotrs9947295
SNPdbers9947295
MSV3drs9947295
GWAS Ctlgrs9947295
GMAF0.1942
Max Magnitude
? (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 8E-6
Odds Ratio NR NR