rs11195062
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11195062(A;A) |
| Make rs11195062(A;C) |
| Make rs11195062(C;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 110277217 |
| Gene | MXI1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11195062 |
| dbSNP (classic) | rs11195062 |
| ClinGen | rs11195062 |
| ebi | rs11195062 |
| HLI | rs11195062 |
| Exac | rs11195062 |
| Gnomad | rs11195062 |
| Varsome | rs11195062 |
| LitVar | rs11195062 |
| Map | rs11195062 |
| PheGenI | rs11195062 |
| Biobank | rs11195062 |
| 1000 genomes | rs11195062 |
| hgdp | rs11195062 |
| ensembl | rs11195062 |
| geneview | rs11195062 |
| scholar | rs11195062 |
| rs11195062 | |
| pharmgkb | rs11195062 |
| gwascentral | rs11195062 |
| openSNP | rs11195062 |
| 23andMe | rs11195062 |
| SNPshot | rs11195062 |
| SNPdbe | rs11195062 |
| MSV3d | rs11195062 |
| GWAS Ctlg | rs11195062 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| 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 | 3E-6 |
| Odds Ratio | 1.13 [NR] |
