List of variants reported as likely pathogenic for mitochondrial complex 2 deficiency, nuclear type 4

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.304G>A (p.Ala102Thr)	rs777578399	0.00003
NM_003000.3(SDHB):c.418G>T (p.Val140Phe)	rs267607032	0.00003
NM_003000.3(SDHB):c.424-1G>A	rs1131691060
NM_003000.3(SDHB):c.589C>T (p.Pro197Ser)	rs2077978300
NM_003000.3(SDHB):c.637dup (p.Met213fs)

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