MSRB3
From SNPedia
| is a | gene |
| is | mentioned by |
| Full name | methionine sulfoxide reductase B3 |
| EntrezGene | 253827 |
| PheGenI | 253827 |
| VariationViewer | 253827 |
| ClinVar | MSRB3 |
| GeneCards | MSRB3 |
| dbSNP | 253827 |
| Diseases | MSRB3 |
| SADR | 253827 |
| HugeNav | 253827 |
| wikipedia | MSRB3 |
| MSRB3 | |
| gopubmed | MSRB3 |
| EVS | MSRB3 |
| HEFalMp | MSRB3 |
| MyGene2 | MSRB3 |
| 23andMe | MSRB3 |
| UniProt | Q8IXL7 |
| Ensembl | ENSG00000174099 |
| OMIM | 613719 |
| # SNPs | 8 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| rs10506525 | 0 | 65,389,598 | |
| rs12229918 | 0 | 65,368,278 | |
| rs149258390 | 0 | 65,308,634 | |
| rs1494508 | 0 | 65,448,478 | |
| rs17178006 | 0 | 65,324,519 | |
| rs201306709 | 0 | 65,368,997 | |
| rs387907088 | 0 | 65,328,584 | |
| rs61921502 | 0 | 65,438,688 |
Associated with deafness; DFNB74
[PMID 25607358] Common genetic variants influence human subcortical brain structures.
