List of variants reported as benign by Center for Human Genetics, Inc, Center for Human Genetics, Inc

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000249.4(MLH1):c.655A>G (p.Ile219Val)	rs1799977	0.23048
NM_000330.4(RS1):c.184+3207C>T	rs35693326	0.02951
NM_000368.5(TSC1):c.1760A>G (p.Lys587Arg)	rs118203576	0.01347
NM_004333.6(BRAF):c.78G>T (p.Glu26Asp)	rs371877084	0.01088
NM_003238.6(TGFB2):c.619G>C (p.Val207Leu)	rs10482810	0.00359
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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