List of variants reported as uncertain significance for encephalopathy due to defective mitochondrial and peroxisomal fission 2

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001277062.2(MFF):c.678A>G (p.Ile226Met)	rs756607883	0.00001
NM_001277062.2(MFF):c.749T>G (p.Ile250Ser)	rs1278600625	0.00001
NM_001277062.2(MFF):c.337C>A (p.Pro113Thr)	rs1414317381
NM_001277062.2(MFF):c.403G>A (p.Val135Ile)
NM_001277062.2(MFF):c.856T>C (p.Trp286Arg)	rs2076297587

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