ClinVar Miner

List of variants in gene combination LOC129929541, SDHB reported as likely benign 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.766-20T>C	rs750144449	0.00001
NM_003000.3(SDHB):c.766-19del	rs1553176985

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