List of variants in gene CDC73 reported as uncertain significance by Sema4, Sema4

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_024529.5(CDC73):c.1031-5C>T	rs746118697	0.00005
NM_024529.5(CDC73):c.1453C>G (p.Leu485Val)	rs761968225	0.00001
NM_024529.5(CDC73):c.1538G>A (p.Arg513Gln)	rs1465509067	0.00001
NM_024529.5(CDC73):c.842G>A (p.Arg281His)	rs762716583	0.00001
NM_024529.5(CDC73):c.1006G>T (p.Ala336Ser)	rs2103178083
NM_024529.5(CDC73):c.29A>T (p.Gln10Leu)	rs2103111611
NM_024529.5(CDC73):c.475G>A (p.Gly159Ser)	rs1675833045

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