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