List of variants reported as likely pathogenic for cardiovascular organ benign neoplasm by Yale Center for Mendelian Genomics, Yale University

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_002253.4(KDR):c.2312C>T (p.Thr771Met)	rs149745504	0.00198
NM_004297.4(GNA14):c.614A>T (p.Gln205Leu)	rs1554685903

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