List of variants in gene CDK4 reported as benign for not provided

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000075.4(CDK4):c.219-31G>A	rs2270777	0.33208
NM_000075.4(CDK4):c.522+41G>A	rs2069502	0.26540
NM_000075.4(CDK4):c.447A>G (p.Thr149=)	rs2069501	0.00639
NM_000075.4(CDK4):c.355-48G>C	rs3211614	0.00380
NM_000075.4(CDK4):c.-60C>G	rs541752163	0.00188
NM_000075.4(CDK4):c.-123T>G	rs759319348	0.00092
NM_000075.4(CDK4):c.522+8G>A	rs758294834	0.00003
NM_000075.4(CDK4):c.549C>T (p.Pro183=)	rs778696237	0.00003
NM_000075.4(CDK4):c.523-4T>A	rs587780667	0.00001
NM_000075.4(CDK4):c.-19-79_-19-78insT	rs2140389055

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