List of variants reported as uncertain significance for Mitochondrial complex 1 deficiency, nuclear type 9

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_004553.6(NDUFS6):c.2T>G (p.Met1Arg)	rs776323741	0.00004
NM_004553.6(NDUFS6):c.247C>T (p.Arg83Trp)	rs863224110	0.00003
NM_004553.6(NDUFS6):c.83T>A (p.Phe28Tyr)	rs905716566	0.00002
NM_004553.6(NDUFS6):c.356T>A (p.Phe119Tyr)	rs2111364938
NM_004553.6(NDUFS6):c.53C>T (p.Ala18Val)
NM_004553.6(NDUFS6):c.92G>T (p.Arg31Leu)	rs770018272

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