List of variants reported as likely benign for intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_006565.4(CTCF):c.1702-10T>C	rs151017109	0.00359
NM_006565.4(CTCF):c.1927C>T (p.Pro643Ser)	rs145727304	0.00312
NM_006565.4(CTCF):c.1962A>C (p.Arg654=)	rs772451262	0.00001
NM_006565.4(CTCF):c.2139C>A (p.Asn713Lys)	rs146712579

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