MYO1A
From SNPedia
| is a | gene |
| is | mentioned by |
| Full name | myosin IA |
| EntrezGene | 4640 |
| PheGenI | 4640 |
| VariationViewer | 4640 |
| ClinVar | MYO1A |
| GeneCards | MYO1A |
| dbSNP | 4640 |
| Diseases | MYO1A |
| SADR | 4640 |
| HugeNav | 4640 |
| wikipedia | MYO1A |
| MYO1A | |
| gopubmed | MYO1A |
| EVS | MYO1A |
| HEFalMp | MYO1A |
| MyGene2 | MYO1A |
| 23andMe | MYO1A |
| UniProt | Q9UBC5 |
| Ensembl | ENSG00000166866 |
| OMIM | 601478 |
| # SNPs | 5 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| rs121909305 | 0 | 57,047,675 | |
| rs121909306 | 0 | 57,029,584 | |
| rs33962952 | 0 | 57,037,618 | |
| rs55679042 | 0 | 57,043,335 | |
| rs61753849 | 0 | 57,041,441 |
Although variants in the MYO1A gene were reported (in 2003) to cause deafness, more recent research (published in 2014 and 2016) concludes that at least so far, all known MYO1A variants do not lead to deafness - they are actually benign.[PMID 24616153],[PMID 27759032]
