List of variants reported as uncertain significance for Hirschsprung disease, susceptibility to, 1; Multiple endocrine neoplasia type 2B; Pheochromocytoma; Familial medullary thyroid carcinoma; Multiple endocrine neoplasia type 2A by Department of Pathology and Laboratory Medicine, Sinai Health System

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2261C>T (p.Thr754Met)	rs181856591	0.00009
NM_020975.6(RET):c.1597G>A (p.Gly533Ser)	rs75873440	0.00008
NM_020975.6(RET):c.1897C>G (p.Leu633Val)	rs267607010	0.00003
NM_020975.6(RET):c.220G>A (p.Gly74Ser)	rs764938319	0.00002
NM_020975.6(RET):c.1462A>T (p.Thr488Ser)	rs753733901	0.00001
NM_020975.6(RET):c.2832C>G (p.Ile944Met)	rs755606269

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