ClinVar Miner

List of variants studied for Inborn mitochondrial myopathy by OMIM

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Total variants: 5
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HGVS dbSNP gnomAD frequency
NC_012920.1(MT-TA):m.5591G>A rs121434458
NC_012920.1(MT-TL2):m.12320A>G rs121434463
NC_012920.1(MT-TM):m.4409T>C rs118203884
NC_012920.1(MT-TW):m.5521G>A rs199474673
NM_001397406.1(FDX2):c.422C>T (p.Pro141Leu) rs888630930

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