List of variants reported as uncertain significance for Mitochondrial inheritance by Department of Pediatrics, Division of Medical Genetics, Faculty of Medicine Ramathibodi Hospital, Mahidol University

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.16159C>A	rs2124599393
NC_012920.1(MT-CYB):m.16182_16183del	rs371240719
NC_012920.1(MT-CYB):m.16230A>G	rs2853514
NC_012920.1(MT-CYB):m.16274G>A	rs144095641
NC_012920.1(MT-CYB):m.16319G>A	rs35105996
NC_012920.1(MT-CYB):m.235A>G	rs3937037
NC_012920.1(MT-CYB):m.249del	rs879043227
NC_012920.1(MT-CYB):m.515AC[4]	rs78907894
NC_012920.1(MT-CYB):m.8272CCCCCTCTA[1]	rs369704279
NC_012920.1(MT-ND1):m.1736A>G	rs193303006
NC_012920.1(MT-ND6):m.14668C>T	rs28357678

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