List of variants in gene SDHA reported as uncertain significance for Gastrointestinal stromal tumor

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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_004168.4(SDHA):c.1663+3G>C	rs751904543	0.00004
NM_004168.4(SDHA):c.512G>A (p.Arg171His)	rs587782076	0.00003
NM_004168.4(SDHA):c.1799G>A (p.Arg600Gln)	rs1126568	0.00002
NM_004168.4(SDHA):c.1754G>A (p.Arg585Gln)	rs752360961	0.00001
NM_004168.4(SDHA):c.511C>T (p.Arg171Cys)	rs776193478	0.00001
NM_004168.4(SDHA):c.923C>T (p.Thr308Met)	rs1457666982	0.00001
NM_004168.4(SDHA):c.1255G>A (p.Gly419Arg)	rs1735709331
NM_004168.4(SDHA):c.1351C>T (p.Arg451Cys)	rs1553999752
NM_004168.4(SDHA):c.1690G>A (p.Glu564Lys)	rs2126633227
NM_004168.4(SDHA):c.698G>T (p.Gly233Val)	rs878854636

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