Variant: rs199474821 

    present in Gene: TRNS1;COX3;COX2;ATP8;COX1;ATP6
    present in Chromosome: MT
    Position on Chromosome: 7511
    Alleles of this Variant: T/C

rs199474821 in TRNS1;COX3;COX2;ATP8;COX1;ATP6 gene and DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL PMID 10371545 1999 Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene.

rs199474821 in TRNS1;COX3;COX2;ATP8;COX1;ATP6 gene and MELAS Syndrome PMID 10371545 1999 Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene.