List of variants in gene CDC73 reported as uncertain significance for CDC73-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: 4

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HGVS	dbSNP	gnomAD frequency
NM_024529.5(CDC73):c.844A>G (p.Thr282Ala)	rs201236330	0.00002
NM_024529.5(CDC73):c.803G>A (p.Arg268Gln)	rs750706815	0.00001
NM_024529.5(CDC73):c.1330G>A (p.Ala444Thr)
NM_024529.5(CDC73):c.746T>C (p.Ile249Thr)	rs973863694

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