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

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.8C>G (p.Ala3Gly)	rs11203289	0.01309
NM_003000.3(SDHB):c.487T>C (p.Ser163Pro)	rs33927012	0.00921
NM_003000.3(SDHB):c.32G>A (p.Arg11His)	rs111430410	0.00185
NM_003000.3(SDHB):c.423+20T>A	rs190139590	0.00179
NM_003000.3(SDHB):c.200+7A>G	rs371329778	0.00005

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