List of variants reported as likely pathogenic for Mitochondrial complex II deficiency, nuclear type 1; Dilated cardiomyopathy 1GG; Paragangliomas 5; Neurodegeneration with ataxia and late-onset optic atrophy by Fulgent Genetics, Fulgent Genetics

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.1432_1432+1del	rs878854627	0.00001
NM_004168.4(SDHA):c.1660C>T (p.Arg554Trp)	rs9809219	0.00001
NM_004168.4(SDHA):c.1663+1G>T	rs766667009	0.00001
NM_004168.4(SDHA):c.1579del (p.Arg527fs)	rs1579437839
NM_004168.4(SDHA):c.1663+1G>A	rs766667009
NM_004168.4(SDHA):c.2T>G (p.Met1Arg)	rs750380279
NM_004168.4(SDHA):c.456+1G>A	rs1579384604
NM_004168.4(SDHA):c.484del (p.Arg162fs)	rs1734988578
NM_004168.4(SDHA):c.688del (p.Glu230fs)	rs1553998199
NM_004168.4(SDHA):c.762_770+17del	rs1041809852

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