rs9272535
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9272535(A;A) |
| Make rs9272535(A;G) |
| Make rs9272535(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32638979 |
| Gene | HLA-DQA1, LOC107986589 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9272535 |
| dbSNP (classic) | rs9272535 |
| ClinGen | rs9272535 |
| ebi | rs9272535 |
| HLI | rs9272535 |
| Exac | rs9272535 |
| Gnomad | rs9272535 |
| Varsome | rs9272535 |
| LitVar | rs9272535 |
| Map | rs9272535 |
| PheGenI | rs9272535 |
| Biobank | rs9272535 |
| 1000 genomes | rs9272535 |
| hgdp | rs9272535 |
| ensembl | rs9272535 |
| geneview | rs9272535 |
| scholar | rs9272535 |
| rs9272535 | |
| pharmgkb | rs9272535 |
| gwascentral | rs9272535 |
| openSNP | rs9272535 |
| 23andMe | rs9272535 |
| SNPshot | rs9272535 |
| SNPdbe | rs9272535 |
| MSV3d | rs9272535 |
| GWAS Ctlg | rs9272535 |
| GMAF | 0.1965 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21131588 ]
|
| Trait | |
| Title | Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL |
| Risk Allele | A |
| P-val | 9E-8 |
| Odds Ratio | 1.6100 [1.35-1.92] |
[PMID 19571809] Common variants on chromosome 6p22.1 are associated with schizophrenia.
[PMID 20485477] New Genetic Findings in Schizophrenia: Is there Still Room for the Dopamine Hypothesis of Schizophrenia?
