rs8056264
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8056264(C;C) |
| Make rs8056264(C;T) |
| Make rs8056264(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 31321334 |
| Gene | ITGAM |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8056264 |
| dbSNP (classic) | rs8056264 |
| ClinGen | rs8056264 |
| ebi | rs8056264 |
| HLI | rs8056264 |
| Exac | rs8056264 |
| Gnomad | rs8056264 |
| Varsome | rs8056264 |
| LitVar | rs8056264 |
| Map | rs8056264 |
| PheGenI | rs8056264 |
| Biobank | rs8056264 |
| 1000 genomes | rs8056264 |
| hgdp | rs8056264 |
| ensembl | rs8056264 |
| geneview | rs8056264 |
| scholar | rs8056264 |
| rs8056264 | |
| pharmgkb | rs8056264 |
| gwascentral | rs8056264 |
| openSNP | rs8056264 |
| 23andMe | rs8056264 |
| SNPshot | rs8056264 |
| SNPdbe | rs8056264 |
| MSV3d | rs8056264 |
| GWAS Ctlg | rs8056264 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
Although based on a relatively small study, there's a strong association (odds ratios above 30) between the very rare (and neighboring) minor alleles of rs8056264 and rs929867 with common variable immunodeficiency (CVID) reported in [PMID 25678086
].
