Variant: rs199730889 

    present in Gene: TRMT10C
    present in Chromosome: 3
    Position on Chromosome: 101565323
    Alleles of this Variant: G/A;T

rs199730889 in TRMT10C gene and COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30 PMID 27132592 2016 Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies.

rs199730889 in TRMT10C gene and Mitochondrial Diseases PMID 27132592 2016 Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies.