Variant: rs1569484151 

    present in Gene: COX1;TRNS1;ATP8;ATP6;COX3;COX2
    present in Chromosome: MT
    Position on Chromosome: 7462
    Alleles of this Variant: C/T

rs1569484151 in COX1;TRNS1;ATP8;ATP6;COX3;COX2 gene and DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL PMID 20722495 2010 Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss.