rs877529
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs877529(C;C) |
| Make rs877529(C;T) |
| Make rs877529(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 39146287 |
| Gene | CBX7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs877529 |
| dbSNP (classic) | rs877529 |
| ClinGen | rs877529 |
| ebi | rs877529 |
| HLI | rs877529 |
| Exac | rs877529 |
| Gnomad | rs877529 |
| Varsome | rs877529 |
| LitVar | rs877529 |
| Map | rs877529 |
| PheGenI | rs877529 |
| Biobank | rs877529 |
| 1000 genomes | rs877529 |
| hgdp | rs877529 |
| ensembl | rs877529 |
| geneview | rs877529 |
| scholar | rs877529 |
| rs877529 | |
| pharmgkb | rs877529 |
| gwascentral | rs877529 |
| openSNP | rs877529 |
| 23andMe | rs877529 |
| SNPshot | rs877529 |
| SNPdbe | rs877529 |
| MSV3d | rs877529 |
| GWAS Ctlg | rs877529 |
| GMAF | 0.3444 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24449210] Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
| GWAS snp | |
|---|---|
| PMID | [PMID 23955597 ]
|
| Trait | Multiple myeloma |
| Title | Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. |
| Risk Allele | A |
| P-val | 8E-16 |
| Odds Ratio | 1.23 [1.17-1.29] |
