rs1049225
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1049225(C;C) |
| Make rs1049225(C;T) |
| Make rs1049225(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 6 |
| Position | 32659970 |
| Gene | HLA-DQB1, HLA-DQB1-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1049225 |
| dbSNP (classic) | rs1049225 |
| ClinGen | rs1049225 |
| ebi | rs1049225 |
| HLI | rs1049225 |
| Exac | rs1049225 |
| Gnomad | rs1049225 |
| Varsome | rs1049225 |
| LitVar | rs1049225 |
| Map | rs1049225 |
| PheGenI | rs1049225 |
| Biobank | rs1049225 |
| 1000 genomes | rs1049225 |
| hgdp | rs1049225 |
| ensembl | rs1049225 |
| geneview | rs1049225 |
| scholar | rs1049225 |
| rs1049225 | |
| pharmgkb | rs1049225 |
| gwascentral | rs1049225 |
| openSNP | rs1049225 |
| 23andMe | rs1049225 |
| SNPshot | rs1049225 |
| SNPdbe | rs1049225 |
| MSV3d | rs1049225 |
| GWAS Ctlg | rs1049225 |
| Max Magnitude | 0 |
778 Common variable immunodeficiency disorder (CVID) cases compared with 10,999 controls using the Illumina Immunochip; confirming the previously reported human leukocyte antigen (HLA) associations on chromosome 6p21. The minor allele, rs1049225(T) as represented on the minus strand, is associated with reduced risk for CVID (odds ratio 0.56, CI: 0.49 - 0.64, p=4.8 × 10e-16).[PMID 25891430
]
