rs9947295
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Make rs9947295(C;C) | 
| Make rs9947295(C;T) | 
| Make rs9947295(T;T) | 
| Reference | GRCh38 38.1/141 | 
| Chromosome | 18 | 
| Position | 11759433 | 
| Gene | GNAL | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs9947295 | 
| dbSNP (classic) | rs9947295 | 
| ClinGen | rs9947295 | 
| ebi | rs9947295 | 
| HLI | rs9947295 | 
| Exac | rs9947295 | 
| Gnomad | rs9947295 | 
| Varsome | rs9947295 | 
| LitVar | rs9947295 | 
| Map | rs9947295 | 
| PheGenI | rs9947295 | 
| Biobank | rs9947295 | 
| 1000 genomes | rs9947295 | 
| hgdp | rs9947295 | 
| ensembl | rs9947295 | 
| geneview | rs9947295 | 
| scholar | rs9947295 | 
| rs9947295 | |
| pharmgkb | rs9947295 | 
| gwascentral | rs9947295 | 
| openSNP | rs9947295 | 
| 23andMe | rs9947295 | 
| SNPshot | rs9947295 | 
| SNPdbe | rs9947295 | 
| MSV3d | rs9947295 | 
| GWAS Ctlg | rs9947295 | 
| GMAF | 0.1942 | 
| Max Magnitude | 0 | 
| ? | (C;C) (C;T) (T;T) | 28 | 
|---|---|---|
| 
 
 | ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23459443  ] | 
| 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 | 
Categories: 
- Is a snp
- In dbSNP
- SNPs on chromosome 18
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d


