List of variants reported as pathogenic for benign neoplasm by MGZ Medical Genetics Center

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.183T>G (p.Tyr61Ter)	rs760169139
NM_003000.3(SDHB):c.3G>A (p.Met1Ile)	rs1131691061

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