rs2473967
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2473967(A;A) |
| Make rs2473967(A;C) |
| Make rs2473967(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 113158133 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2473967 |
| dbSNP (classic) | rs2473967 |
| ClinGen | rs2473967 |
| ebi | rs2473967 |
| HLI | rs2473967 |
| Exac | rs2473967 |
| Gnomad | rs2473967 |
| Varsome | rs2473967 |
| LitVar | rs2473967 |
| Map | rs2473967 |
| PheGenI | rs2473967 |
| Biobank | rs2473967 |
| 1000 genomes | rs2473967 |
| hgdp | rs2473967 |
| ensembl | rs2473967 |
| geneview | rs2473967 |
| scholar | rs2473967 |
| rs2473967 | |
| pharmgkb | rs2473967 |
| gwascentral | rs2473967 |
| openSNP | rs2473967 |
| 23andMe | rs2473967 |
| SNPshot | rs2473967 |
| SNPdbe | rs2473967 |
| MSV3d | rs2473967 |
| GWAS Ctlg | rs2473967 |
| GMAF | 0.1162 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | 2E-6 |
| Odds Ratio | NR NR |
