List of variants in gene SDHB reported as uncertain significance for Pheochromocytoma

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.440A>G (p.Tyr147Cys)	rs774568101	0.00010
NM_003000.3(SDHB):c.307A>G (p.Met103Val)	rs140178341	0.00004
NM_003000.3(SDHB):c.47C>G (p.Thr16Arg)	rs775350144	0.00001
NM_003000.2(SDHB):c.-81G>T	rs886045586
NM_003000.2(SDHB):c.424-16_424-14dup	rs34261028
NM_003000.3(SDHB):c.424-37TTC[6]	rs34261028
NM_003000.3(SDHB):c.662A>G (p.Asp221Gly)	rs2101513961
NM_003000.3(SDHB):c.716C>G (p.Ser239Cys)	rs201098090
NM_003000.3(SDHB):c.79C>G (p.Arg27Gly)	rs74315369

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