List of variants in gene SDHA reported as likely benign for Leigh syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_004168.3(SDHA):c.-115T>C	rs2303741	0.25160
NM_004168.4(SDHA):c.1680G>A (p.Thr560=)	rs1139449	0.25156
NM_004168.4(SDHA):c.1886A>T (p.Tyr629Phe)	rs6960	0.24550
NM_004168.4(SDHA):c.1908+15C>T	rs34504623	0.08152
NM_004168.4(SDHA):c.549C>T (p.Gly183=)	rs61733344	0.00892
NM_004168.4(SDHA):c.969C>T (p.Gly323=)	rs142849100	0.00430
NM_004168.4(SDHA):c.1623G>A (p.Lys541=)	rs35502109	0.00206
NM_004168.4(SDHA):c.550G>A (p.Gly184Arg)	rs148246073	0.00056
NM_004168.4(SDHA):c.163T>C (p.Tyr55His)	rs142926807	0.00046
NM_004168.3(SDHA):c.-84dup	rs35805262

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