ClinVar Miner

List of variants in gene CDC73 reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_024529.5(CDC73):c.*2420A>C	rs536960020	0.00010
NM_024529.5(CDC73):c.*1144dup	rs538761780

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