Gene: GPSM2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 29899
Gene Symbol: GPSM2
GPSM2 		0.010 GeneticVariation disease BEFREE Mutations in GPSM2 have been previously identified in people with profound congenital nonsyndromic hearing loss (NSHL). 22578326 2012