Variant: rs118192099 

    present in Gene: ATP6;COX3;ND3;COX2;TRNK;ATP8
    present in Chromosome: MT
    Position on Chromosome: 8356
    Alleles of this Variant: T/C

rs118192099 in ATP6;COX3;ND3;COX2;TRNK;ATP8 gene and MELAS Syndrome PMID 1361099 1992 A new mtDNA mutation in the tRNA(Lys) gene associated with myoclonic epilepsy and ragged-red fibers (MERRF).