List of variants in gene CCDC39 reported as likely pathogenic for CCDC39-related 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_181426.2(CCDC39):c.1874G>T (p.Ser625Ile)	rs769223754	0.00005
NM_181426.2(CCDC39):c.1073_1076del (p.Thr358fs)	rs878855279
NM_181426.2(CCDC39):c.610_613del	rs1415346246

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