List of variants in gene SDHA reported as benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.891T>C (p.Pro297=)	rs1126417	0.74998
NM_004168.4(SDHA):c.1932G>A (p.Val644=)	rs6961	0.26598
NM_004168.4(SDHA):c.619A>C (p.Arg207=)	rs6555055	0.25190
NM_004168.4(SDHA):c.684T>C (p.Asn228=)	rs2115272	0.25174
NM_004168.4(SDHA):c.1886A>T (p.Tyr629Phe)	rs6960	0.24550
NM_004168.4(SDHA):c.113A>T (p.Asp38Val)	rs34635677	0.02888
NM_004168.4(SDHA):c.1664-8G>A	rs199790689	0.01533
NM_004168.4(SDHA):c.1305G>T (p.Leu435=)	rs35964044	0.01515
NM_004168.4(SDHA):c.822C>T (p.Gly274=)	rs34771391	0.01114
NM_004168.4(SDHA):c.549C>T (p.Gly183=)	rs61733344	0.00892
NM_004168.4(SDHA):c.456+20G>C	rs193283468	0.00385
NM_004168.4(SDHA):c.1911C>T (p.Val637=)	rs11557098	0.00180
NM_004168.4(SDHA):c.771-11A>G	rs2288461

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