List of variants in gene SDHB reported as benign for Gastrointestinal stromal tumor

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.201-36G>T	rs1022580	0.95416
NM_003000.3(SDHB):c.18C>A (p.Ala6=)	rs2746462	0.95374
NM_003000.3(SDHB):c.73-21G>T	rs1311107626

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