rs11766496
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11766496(C;C) |
Make rs11766496(C;G) |
Make rs11766496(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 71923865 |
Gene | CALN1 |
is a | snp |
is | mentioned by |
dbSNP | rs11766496 |
dbSNP (classic) | rs11766496 |
ClinGen | rs11766496 |
ebi | rs11766496 |
HLI | rs11766496 |
Exac | rs11766496 |
Gnomad | rs11766496 |
Varsome | rs11766496 |
LitVar | rs11766496 |
Map | rs11766496 |
PheGenI | rs11766496 |
Biobank | rs11766496 |
1000 genomes | rs11766496 |
hgdp | rs11766496 |
ensembl | rs11766496 |
geneview | rs11766496 |
scholar | rs11766496 |
rs11766496 | |
pharmgkb | rs11766496 |
gwascentral | rs11766496 |
openSNP | rs11766496 |
23andMe | rs11766496 |
SNPshot | rs11766496 |
SNPdbe | rs11766496 |
MSV3d | rs11766496 |
GWAS Ctlg | rs11766496 |
GMAF | 0.1304 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22837378] |
Trait | Airflow obstruction |
Title | Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. |
Risk Allele | C |
P-val | 2E-6 |
Odds Ratio | 1.30 |