List of variants reported as uncertain significance for Hereditary pheochromocytoma-paraganglioma by Section on Medical Neuroendocrinolgy, National Institutes of Health

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_003002.4(SDHD):c.479G>T (p.Ter160Leu)	rs201372601	0.00002
NM_003000.3(SDHB):c.445C>T (p.Gln149Ter)	rs876658451
NM_003000.3(SDHB):c.642G>C (p.Gln214His)	rs1278834014
NM_003001.5(SDHC):c.218G>A (p.Gly73Asp)	rs1553264219
NM_003002.4(SDHD):c.148C>G (p.His50Asp)	rs779249550
NM_003002.4(SDHD):c.239T>G (p.Leu80Arg)	rs1555187010
NM_003002.4(SDHD):c.328GTT[1] (p.Val111del)	rs1555187580
NM_003002.4(SDHD):c.443G>T (p.Gly148Val)	rs1555187633

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