List of variants in gene SDHB reported as likely pathogenic by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.143A>T (p.Asp48Val)	rs202101384	0.00001
NM_003000.3(SDHB):c.649C>T (p.Arg217Cys)	rs200245469	0.00001
NM_003000.3(SDHB):c.689G>A (p.Arg230His)	rs587782604	0.00001
NM_003000.3(SDHB):c.416T>C (p.Leu139Pro)

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