List of variants reported as uncertain significance for connective tissue neoplasm by Equipe Genetique des Anomalies du Developpement, Université de Bourgogne

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004716.4(PCSK7):c.1678C>G (p.Arg560Gly)	rs202038275	0.00023
NM_004716.4(PCSK7):c.1634A>C (p.Lys545Thr)	rs771986131	0.00001
NM_001374353.1(GLI2):c.3784C>T (p.His1262Tyr)	rs794727100

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