ClinVar Miner

List of variants reported as pathogenic for paragangliomas 4 by Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine

Included ClinVar conditions (6):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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.79C>T (p.Arg27Ter)	rs74315369	0.00003
NM_003000.3(SDHB):c.688C>T (p.Arg230Cys)	rs138996609	0.00001

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