rs9296092
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9296092(A;A) |
Make rs9296092(A;G) |
Make rs9296092(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 33510719 |
Gene | SYNGAP1 |
is a | snp |
is | mentioned by |
dbSNP | rs9296092 |
dbSNP (classic) | rs9296092 |
ClinGen | rs9296092 |
ebi | rs9296092 |
HLI | rs9296092 |
Exac | rs9296092 |
Gnomad | rs9296092 |
Varsome | rs9296092 |
LitVar | rs9296092 |
Map | rs9296092 |
PheGenI | rs9296092 |
Biobank | rs9296092 |
1000 genomes | rs9296092 |
hgdp | rs9296092 |
ensembl | rs9296092 |
geneview | rs9296092 |
scholar | rs9296092 |
rs9296092 | |
pharmgkb | rs9296092 |
gwascentral | rs9296092 |
openSNP | rs9296092 |
23andMe | rs9296092 |
SNPshot | rs9296092 |
SNPdbe | rs9296092 |
MSV3d | rs9296092 |
GWAS Ctlg | rs9296092 |
GMAF | 0.3783 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21685187] |
Trait | |
Title | Genome-wide association study of smoking behaviours in patients with COPD. |
Risk Allele | |
P-val | 6E-7 |
Odds Ratio | None [NR] |
[PMID 26502206] Association of multiple genetic variants with chronic obstructive pulmonary disease (COPD) susceptibility in Hainan region
[PMID 32234053] Comparison and development of machine learning tools for the prediction of chronic obstructive pulmonary disease in the Chinese population.