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81460 - mitochondrial genome with heteroplasmy detection

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Procedure / Servicemitochondrial genome with heteroplasmy detection
Procedure / Service Description

Genetic testing for severe inherited conditions (eg, cystic fibrosis, Ashkenazi Jewish- - [MERFF], neuropathy, ataxia, and retinitis pigmentosa [NARP], Leber hereditary optic neuropathy [LHON]), genomic sequence, must include sequence analysis of entire 81460 mitochondrial genome with heteroplasmy detection Solid organ neoplasm, genomic sequence analysis panel, cell-free nucleic acid (eg, plasma), interrogation for sequence variants; DNA analysis or combined DNA and RNA analysis, copy

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  • Submit clinical notes if requested by the plan
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