List of variants in gene SDHA reported as likely pathogenic for not provided

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.1A>G (p.Met1Val)	rs1061517	0.00013
NM_004168.4(SDHA):c.1751C>T (p.Ala584Val)	rs201068049	0.00009
NM_004168.4(SDHA):c.1534C>T (p.Arg512Ter)	rs748089700	0.00005
NM_004168.4(SDHA):c.1526C>G (p.Ser509Trp)	rs397514541	0.00004
NM_004168.4(SDHA):c.223C>T (p.Arg75Ter)	rs781764920	0.00003
NM_004168.4(SDHA):c.1765C>T (p.Arg589Trp)	rs387906780	0.00002
NM_004168.4(SDHA):c.1471G>T (p.Glu491Ter)	rs778207102	0.00001
NM_004168.4(SDHA):c.150+1G>A	rs1057523165	0.00001
NM_004168.4(SDHA):c.1660C>T (p.Arg554Trp)	rs9809219	0.00001
NM_004168.4(SDHA):c.1753C>T (p.Arg585Trp)	rs200397144	0.00001
NM_004168.4(SDHA):c.1885dup (p.Tyr629fs)	rs750865703	0.00001
NM_004168.4(SDHA):c.778G>A (p.Gly260Arg)	rs940845256	0.00001
NM_004168.4(SDHA):c.923C>T (p.Thr308Met)	rs1457666982	0.00001
NM_004168.4(SDHA):c.1054del (p.Arg352fs)
NM_004168.4(SDHA):c.1260+2T>A	rs1735710103
NM_004168.4(SDHA):c.1351C>T (p.Arg451Cys)	rs1553999752
NM_004168.4(SDHA):c.1468G>T (p.Glu490Ter)	rs1554000360
NM_004168.4(SDHA):c.171dup (p.Val58fs)	rs1553997323
NM_004168.4(SDHA):c.1729C>T (p.Gln577Ter)
NM_004168.4(SDHA):c.1866G>A (p.Trp622Ter)	rs1579445179
NM_004168.4(SDHA):c.1A>T (p.Met1Leu)	rs1061517
NM_004168.4(SDHA):c.242_243insA (p.Ser81_Glu82insTer)	rs2126542910
NM_004168.4(SDHA):c.255del (p.Phe85fs)	rs760710175
NM_004168.4(SDHA):c.378del (p.Thr126_Val127insTer)	rs1553997617
NM_004168.4(SDHA):c.46_52dup (p.Leu18fs)	rs1560980939
NM_004168.4(SDHA):c.554dup (p.Ala186fs)	rs1173940446
NM_004168.4(SDHA):c.559del (p.His187fs)	rs2126550020
NM_004168.4(SDHA):c.786del (p.Tyr263fs)	rs1553998613

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