List of variants reported as likely pathogenic for Mitochondrial complex 1 deficiency, nuclear type 19

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_017547.4(FOXRED1):c.920G>A (p.Gly307Glu)	rs145888229	0.00016
NM_017547.4(FOXRED1):c.406C>T (p.Arg136Trp)	rs373075574	0.00001
NM_017547.4(FOXRED1):c.86-1G>A	rs768720209	0.00001
NM_017547.4(FOXRED1):c.1057G>T (p.Glu353Ter)	rs780131344
NM_017547.4(FOXRED1):c.209G>C (p.Gly70Ala)	rs1950986906
NM_017547.4(FOXRED1):c.733+1G>A

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