List of variants reported as pathogenic for congenital heart defects, dysmorphic facial features, and intellectual developmental disorder by OMIM

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_003718.5(CDK13):c.2140G>C (p.Gly714Arg)	rs1057519633
NM_003718.5(CDK13):c.2149G>A (p.Gly717Arg)	rs1057519632
NM_003718.5(CDK13):c.2252G>A (p.Arg751Gln)	rs1057519634
NM_003718.5(CDK13):c.2524A>G (p.Asn842Asp)	rs1554333853
NM_003718.5(CDK13):c.2525A>G (p.Asn842Ser)	rs878853160
NM_003718.5(CDK13):c.2620G>T (p.Val874Leu)

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