List of variants in gene SDHC reported as likely pathogenic 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_003001.5(SDHC):c.377A>G (p.Tyr126Cys)	rs898854295	0.00003
NM_003001.5(SDHC):c.148C>T (p.Arg50Cys)	rs587778661	0.00001
NM_003001.5(SDHC):c.215G>A (p.Arg72His)	rs778582853	0.00001
NM_003001.5(SDHC):c.380A>G (p.His127Arg)	rs786203457	0.00001
NM_003001.5(SDHC):c.179+1G>T	rs1057517818
NM_003001.5(SDHC):c.387G>A (p.Trp129Ter)	rs981049067

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