List of variants in gene combination CDK13, LOC129998292 reported as uncertain significance for Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003718.5(CDK13):c.218C>T (p.Ala73Val)	rs1021210496
NM_003718.5(CDK13):c.482G>T (p.Gly161Val)
NM_003718.5(CDK13):c.484dup (p.Ala162fs)	rs1405252481

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