rs10669586
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10669586(-;-) |
| Make rs10669586(-;CT) |
| Make rs10669586(CT;CT) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 10 |
| Position | 46046600 |
| Gene | MSMB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10669586 |
| dbSNP (classic) | rs10669586 |
| ClinGen | rs10669586 |
| ebi | rs10669586 |
| HLI | rs10669586 |
| Exac | rs10669586 |
| Gnomad | rs10669586 |
| Varsome | rs10669586 |
| LitVar | rs10669586 |
| Map | rs10669586 |
| PheGenI | rs10669586 |
| Biobank | rs10669586 |
| 1000 genomes | rs10669586 |
| hgdp | rs10669586 |
| ensembl | rs10669586 |
| geneview | rs10669586 |
| scholar | rs10669586 |
| rs10669586 | |
| pharmgkb | rs10669586 |
| gwascentral | rs10669586 |
| openSNP | rs10669586 |
| 23andMe | rs10669586 |
| SNPshot | rs10669586 |
| SNPdbe | rs10669586 |
| MSV3d | rs10669586 |
| GWAS Ctlg | rs10669586 |
| Max Magnitude | 0 |
[PMID 26240778
] The rs10993994 in the proximal MSMB promoter region is a functional polymorphism in Asian Indian subjects
