List of variants reported as pathogenic for multiple congenital anomalies/dysmorphic syndrome by Cavalleri Lab, Royal College of Surgeons in Ireland

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_007059.4(KPTN):c.597_598dup (p.Ser200fs)	rs766372684	0.00010
NM_013275.6(ANKRD11):c.7571A>G (p.Glu2524Gly)	rs2033513257

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