List of variants reported as likely benign 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2988G>A (p.Pro996=)	rs145798106	0.00013
NM_020975.6(RET):c.582G>A (p.Gln194=)	rs368116579	0.00003
NM_020975.6(RET):c.1920C>T (p.Ala640=)	rs149768519	0.00001
NM_020975.6(RET):c.279C>A (p.Gly93=)	rs1168926729

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