List of variants reported as uncertain significance for Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency by Fulgent Genetics, Fulgent Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_012123.4(MTO1):c.1129+246G>A	rs118010902	0.00049
NM_012123.4(MTO1):c.1222A>G (p.Ile408Val)	rs149407452	0.00004
NM_012123.4(MTO1):c.514C>T (p.Arg172Cys)	rs370046018	0.00003
NM_012123.4(MTO1):c.535+5G>A	rs1405997705	0.00001
NM_012123.4(MTO1):c.1393A>G (p.Met465Val)	rs1000432861
NM_012123.4(MTO1):c.605T>C (p.Val202Ala)	rs1206431304

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