List of variants reported as pathogenic for cardiovascular organ benign 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_000492.4(CFTR):c.2490+2T>C	rs1057516216	0.00001
NM_005633.4(SOS1):c.1300G>A (p.Gly434Arg)	rs397517148
NM_006767.4(LZTR1):c.742G>A (p.Gly248Arg)	rs869320686

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