Variant: rs1131692056 

    present in Gene: PRKCB
    present in Chromosome: 16
    Position on Chromosome: 23988577
    Alleles of this Variant: G/T

rs1131692056 in PRKCB gene and Sensorineural Hearing Loss (disorder) PMID 27329761 2016 A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease.