"All of Us Research Program, National Institutes of Health"[submitter] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 849934	NM_003000.3(SDHB):c.72G>C (p.Gln24His)	LOC129929542, SDHB (Q24H)	Single nucleotide variant (missense variant)	Hereditary pheochromocytoma-paraganglioma +3 more	GUncertain significance
Select item 528740	NM_003000.3(SDHB):c.72G>A (p.Gln24=)	LOC129929542, SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +3 more	GConflicting classifications of pathogenicity
Select item 239439	NM_003000.3(SDHB):c.71A>C (p.Gln24Pro)	LOC129929542, SDHB (Q24P)	Single nucleotide variant (missense variant)	Hereditary pheochromocytoma-paraganglioma +4 more	GUncertain significance
Select item 452783	NM_003000.3(SDHB):c.67C>G (p.Leu23Val)	LOC129929542, SDHB (L23V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GUncertain significance
Select item 486426	NM_003000.3(SDHB):c.66C>T (p.Cys22=)	LOC129929542, SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +4 more	GLikely benign
Select item 528742	NM_003000.3(SDHB):c.65G>A (p.Cys22Tyr)	LOC129929542, SDHB (C22Y)	Single nucleotide variant (missense variant)	Pheochromocytoma +4 more	GUncertain significance
Select item 459163	NM_003000.3(SDHB):c.65G>T (p.Cys22Phe)	LOC129929542, SDHB (C22F)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +6 more	GUncertain significance
Select item 3070294	NM_003000.3(SDHB):c.62C>A (p.Ala21Asp)	LOC129929542, SDHB (A21D)	Single nucleotide variant (missense variant)	Hereditary pheochromocytoma-paraganglioma	GUncertain significance