List of variants reported as benign for multiple congenital anomalies/dysmorphic syndrome by Center for Human Genetics, Inc, Center for Human Genetics, Inc

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.78G>T (p.Glu26Asp)	rs371877084	0.01088
NM_022455.5(NSD1):c.4520C>T (p.Thr1507Met)	rs144900277	0.00206
NM_017780.4(CHD7):c.1565G>T (p.Gly522Val)	rs142962579	0.00101
NM_003482.4(KMT2D):c.4724T>C (p.Met1575Thr)	rs1555194803

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