ClinVar Miner

List of variants in gene SDHB reported as likely pathogenic by Genetics and Molecular Pathology, SA Pathology

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.649C>T (p.Arg217Cys)	rs200245469	0.00001
NM_003000.3(SDHB):c.572G>A (p.Cys191Tyr)	rs2077978456

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