List of variants reported as uncertain significance for Mitochondrial complex 1 deficiency, nuclear type 5 by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_005006.7(NDUFS1):c.-5+236T>C	rs184505364	0.00195
NM_005006.7(NDUFS1):c.908C>G (p.Thr303Ser)	rs75666426	0.00016
NM_005006.7(NDUFS1):c.*27C>T	rs369746514	0.00012
NM_005006.7(NDUFS1):c.325T>A (p.Ser109Thr)	rs769616417	0.00007

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