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;