rs1047992
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1047992(A;A) |
| Make rs1047992(A;G) |
| Make rs1047992(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 6 |
| Position | 32637489 |
| Gene | HLA-DQA1, LOC107986589 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1047992 |
| dbSNP (classic) | rs1047992 |
| ClinGen | rs1047992 |
| ebi | rs1047992 |
| HLI | rs1047992 |
| Exac | rs1047992 |
| Gnomad | rs1047992 |
| Varsome | rs1047992 |
| LitVar | rs1047992 |
| Map | rs1047992 |
| PheGenI | rs1047992 |
| Biobank | rs1047992 |
| 1000 genomes | rs1047992 |
| hgdp | rs1047992 |
| ensembl | rs1047992 |
| geneview | rs1047992 |
| scholar | rs1047992 |
| rs1047992 | |
| pharmgkb | rs1047992 |
| gwascentral | rs1047992 |
| openSNP | rs1047992 |
| 23andMe | rs1047992 |
| SNPshot | rs1047992 |
| SNPdbe | rs1047992 |
| MSV3d | rs1047992 |
| GWAS Ctlg | rs1047992 |
| Max Magnitude | 0 |
[PMID 30006974
] Association of HLA-DQA1 gene polymorphisms with the risk of children primary nephrotic syndrome in Chinese population.
