rs226088
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs226088(C;C) |
| Make rs226088(C;T) |
| Make rs226088(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 17 |
| Position | 35690325 |
| Gene | AP2B1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs226088 |
| dbSNP (classic) | rs226088 |
| ClinGen | rs226088 |
| ebi | rs226088 |
| HLI | rs226088 |
| Exac | rs226088 |
| Gnomad | rs226088 |
| Varsome | rs226088 |
| LitVar | rs226088 |
| Map | rs226088 |
| PheGenI | rs226088 |
| Biobank | rs226088 |
| 1000 genomes | rs226088 |
| hgdp | rs226088 |
| ensembl | rs226088 |
| geneview | rs226088 |
| scholar | rs226088 |
| rs226088 | |
| pharmgkb | rs226088 |
| gwascentral | rs226088 |
| openSNP | rs226088 |
| 23andMe | rs226088 |
| SNPshot | rs226088 |
| SNPdbe | rs226088 |
| MSV3d | rs226088 |
| GWAS Ctlg | rs226088 |
| GMAF | 0.3994 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19728873
] Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions
