rs17806056
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17806056(A;A) |
| Make rs17806056(A;T) |
| Make rs17806056(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 11098642 |
| Gene | CLEC16A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17806056 |
| dbSNP (classic) | rs17806056 |
| ClinGen | rs17806056 |
| ebi | rs17806056 |
| HLI | rs17806056 |
| Exac | rs17806056 |
| Gnomad | rs17806056 |
| Varsome | rs17806056 |
| LitVar | rs17806056 |
| Map | rs17806056 |
| PheGenI | rs17806056 |
| Biobank | rs17806056 |
| 1000 genomes | rs17806056 |
| hgdp | rs17806056 |
| ensembl | rs17806056 |
| geneview | rs17806056 |
| scholar | rs17806056 |
| rs17806056 | |
| pharmgkb | rs17806056 |
| gwascentral | rs17806056 |
| openSNP | rs17806056 |
| 23andMe | rs17806056 |
| SNPshot | rs17806056 |
| SNPdbe | rs17806056 |
| MSV3d | rs17806056 |
| GWAS Ctlg | rs17806056 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
778 Common variable immunodeficiency disorder (CVID) cases compared with 10,999 controls using the Illumina Immunochip; the first non-HLA genome-wide significant risk for CVID locus was found within the CLEC16A gene, namely rs17806056. The minor allele, rs17806056(A), is associated with reduced risk for CVID (odds ratio 0.66, CI: 0.57 - 0.75, p=2.0 × 10e-9).[PMID 25891430
]
