List of variants in gene SDHA reported as benign by Sema4, Sema4

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.684T>C (p.Asn228=)	rs2115272	0.25174
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.146A>G (p.Asp49Gly)	rs80207011	0.00261
NM_004168.4(SDHA):c.1523C>T (p.Thr508Ile)	rs151266052	0.00245
NM_004168.4(SDHA):c.1368G>A (p.Ser456=)	rs149875171	0.00117
NM_004168.4(SDHA):c.1002G>A (p.Ala334=)	rs144252500	0.00075
NM_004168.4(SDHA):c.600A>G (p.Leu200=)	rs201967413	0.00056
NM_004168.4(SDHA):c.723C>T (p.Asp241=)	rs146653693	0.00049
NM_004168.4(SDHA):c.163T>C (p.Tyr55His)	rs142926807	0.00046
NM_004168.4(SDHA):c.895+13G>A	rs201461936	0.00025
NM_004168.4(SDHA):c.1569T>C (p.Ala523=)	rs150192376	0.00019
NM_004168.4(SDHA):c.918C>G (p.Leu306=)	rs138828792	0.00017
NM_004168.4(SDHA):c.1527G>A (p.Ser509=)	rs746453879	0.00008
NM_004168.4(SDHA):c.597G>A (p.Ser199=)	rs141874250	0.00002
NM_004168.4(SDHA):c.825C>T (p.Asp275=)	rs1237373391	0.00002
NM_004168.4(SDHA):c.1344T>C (p.Gly448=)	rs551497992

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