| is a | gene |
| is | mentioned by |
| Full name | Usher syndrome 1G (autosomal recessive) |
| Other names | SANS |
| EntrezGene | 124590 |
| PheGenI | 124590 |
| VariationViewer | 124590 |
| ClinVar | USH1G |
| GeneCards | USH1G |
| dbSNP | 124590 |
| Diseases | USH1G |
| SADR | 124590 |
| HugeNav | 124590 |
| wikipedia | USH1G |
| USH1G | |
| gopubmed | USH1G |
| EVS | USH1G |
| HEFalMp | USH1G |
| MyGene2 | USH1G |
| 23andMe | USH1G |
| UniProt | Q495M9 |
| Ensembl | ENSG00000182040 |
| OMIM | 607696 |
| # SNPs | 8 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| rs104894651 | 0 | 74,922,931 | |
| rs104894652 | 0 | 74,922,961 | |
| rs397515345 | 0 | 74,919,985 | |
| rs397517925 | 5 | 74,919,463 | |
| rs587776546 | 0 | 74,920,441 | |
| rs730880268 | 0 | 74,920,649 | |
| rs876657419 | 0 | 74,923,028 | |
| rs886043626 | 0 | 74,919,525 |
Associated with deafness;
