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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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP
NM_001374353.1(GLI2):c.3784C>T (p.His1262Tyr)
NM_004716.4(PCSK7):c.1634A>C (p.Lys545Thr)
NM_004716.4(PCSK7):c.1678C>G (p.Arg560Gly)

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