List of variants in gene SDHB reported as benign by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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.18C>A (p.Ala6=)	rs2746462	0.95374
NM_003000.3(SDHB):c.487T>C (p.Ser163Pro)	rs33927012	0.00921
NM_003000.3(SDHB):c.24C>T (p.Ser8=)	rs148738139	0.00461
NM_003000.3(SDHB):c.21C>T (p.Leu7=)	rs147815442	0.00050

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