List of variants in gene SDHB reported as likely pathogenic by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.137G>A (p.Arg46Gln)	rs772551056	0.00001
NM_003000.3(SDHB):c.260T>C (p.Leu87Ser)	rs727504457
NM_003000.3(SDHB):c.287-1G>C	rs397516833
NM_003000.3(SDHB):c.445_446insTATGG (p.Gln149fs)	rs1553177688
NM_003000.3(SDHB):c.575G>C (p.Cys192Ser)	rs397516835
NM_003000.3(SDHB):c.600G>A (p.Trp200Ter)	rs397516836

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