Gene: MYO15A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51168
Gene Symbol: MYO15A
MYO15A 		0.020 GeneticVariation disease BEFREE MYO15A variants are responsible for human non-syndromic autosomal recessive deafness (DFNB3). 30953472 2019
Entrez Id: 51168
Gene Symbol: MYO15A
MYO15A 		0.020 Biomarker disease BEFREE This critical region lies within the CMT type 1A duplication region and excludes MYO15, a gene coding an unconventional myosin that causes a form of autosomal recessive deafness called DFNB3. 10330345 1999