List of variants in gene CDC73 reported as benign by GeneDx

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_024529.5(CDC73):c.1155-122C>G	rs10921328	0.62038
NM_024529.5(CDC73):c.423+108G>A	rs10921318	0.60647
NM_024529.5(CDC73):c.1418-67T>G	rs41305084	0.05617
NM_024529.5(CDC73):c.908-216G>A	rs74130925	0.04519
NM_024529.5(CDC73):c.1067-108T>G	rs41308389	0.04426
NM_024529.5(CDC73):c.1317-335T>G	rs74130938	0.04401
NM_024529.5(CDC73):c.729+61T>A	rs79598234	0.02240
NM_024529.5(CDC73):c.1067-86C>T	rs41302543	0.01942
NM_024529.5(CDC73):c.828+29A>T	rs138541554	0.01151
NM_024529.5(CDC73):c.1185A>G (p.Gln395=)	rs116358657	0.00511
NC_000001.11:g.193121735C>A	rs10737621
NM_024529.5(CDC73):c.-4dup	rs545666726
NM_024529.5(CDC73):c.1030+44G>A	rs74920792
NM_024529.5(CDC73):c.1154+144A>T	rs115158706
NM_024529.5(CDC73):c.1317-114T>A	rs3738244
NM_024529.5(CDC73):c.1418-17C>G	rs11583414
NM_024529.5(CDC73):c.237+28T>C	rs4466634
NM_024529.5(CDC73):c.237+29_237+32del	rs80356645
NM_024529.5(CDC73):c.423+297dup	rs1038256301

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