List of variants in gene SDHA reported as pathogenic by GeneDx

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.91C>T (p.Arg31Ter)	rs142441643	0.00025
NM_004168.4(SDHA):c.1A>G (p.Met1Val)	rs1061517	0.00013
NM_004168.4(SDHA):c.1534C>T (p.Arg512Ter)	rs748089700	0.00005
NM_004168.4(SDHA):c.223C>T (p.Arg75Ter)	rs781764920	0.00003
NM_004168.4(SDHA):c.1151C>G (p.Ser384Ter)	rs151170408	0.00001
NM_004168.4(SDHA):c.1432_1432+1del	rs878854627	0.00001
NM_004168.4(SDHA):c.1663+1G>T	rs766667009	0.00001
NM_004168.4(SDHA):c.553C>T (p.Gln185Ter)	rs775827529	0.00001
NM_004168.4(SDHA):c.1526_1527delinsGA (p.Ser509Ter)	rs1064793567
NM_004168.4(SDHA):c.1571C>T (p.Ala524Val)	rs137852767
NM_004168.4(SDHA):c.160C>T (p.Gln54Ter)	rs1560985916
NM_004168.4(SDHA):c.1del (p.Met1fs)	rs1085307796
NM_004168.4(SDHA):c.2T>G (p.Met1Arg)	rs750380279
NM_004168.4(SDHA):c.356G>A (p.Trp119Ter)	rs1734957331
NM_004168.4(SDHA):c.667del (p.Asp223fs)	rs587782077
NM_004168.4(SDHA):c.688del (p.Glu230fs)	rs1553998199
NM_004168.4(SDHA):c.990del (p.Arg329_Tyr330insTer)	rs886041867
NM_004168.4(SDHA):c.995_996del (p.Pro332fs)	rs1560994766

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