rs16929097
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common genotype |
| Make rs16929097(A;A) |
| Make rs16929097(A;G) |
| Reference | GRCh37.p10 37.5/138 |
| Chromosome | 9 |
| Position | 12521826 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16929097 |
| dbSNP (classic) | rs16929097 |
| ClinGen | rs16929097 |
| ebi | rs16929097 |
| HLI | rs16929097 |
| Exac | rs16929097 |
| Gnomad | rs16929097 |
| Varsome | rs16929097 |
| LitVar | rs16929097 |
| Map | rs16929097 |
| PheGenI | rs16929097 |
| Biobank | rs16929097 |
| 1000 genomes | rs16929097 |
| hgdp | rs16929097 |
| ensembl | rs16929097 |
| geneview | rs16929097 |
| scholar | rs16929097 |
| rs16929097 | |
| pharmgkb | rs16929097 |
| gwascentral | rs16929097 |
| openSNP | rs16929097 |
| 23andMe | rs16929097 |
| SNPshot | rs16929097 |
| SNPdbe | rs16929097 |
| MSV3d | rs16929097 |
| GWAS Ctlg | rs16929097 |
| GMAF | 0.04178 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23829686 ]
|
| Trait | Asthma (childhood onset) |
| Title | Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations. |
| Risk Allele | |
| P-val | 8E-9 |
| Odds Ratio | NR NR |
