Variant: rs794728016 

    present in Gene: MET
    present in Chromosome: 7
    Position on Chromosome: 116763206
    Alleles of this Variant: T/G

rs794728016 in MET gene and Severe hearing loss PMID 25941349 2015 A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss.