List of variants reported as likely pathogenic for Snijders Blok-Campeau syndrome by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001005273.3(CHD3):c.5007_5008del (p.Asp1671fs)	rs967826828	0.00001
NM_001005273.3(CHD3):c.1888T>C (p.Trp630Arg)	rs2151542224
NM_001005273.3(CHD3):c.3020T>G (p.Leu1007Trp)
NM_001005273.3(CHD3):c.3416G>A (p.Gly1139Glu)
NM_001005273.3(CHD3):c.3512A>G (p.His1171Arg)	rs1567861489
NM_001005273.3(CHD3):c.5663G>A (p.Arg1888Gln)

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