List of variants in gene combination CDK4, LOC130008148 reported as likely benign by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000075.4(CDK4):c.141A>C (p.Gly47=)	rs863224320	0.00001
NM_000075.4(CDK4):c.180G>A (p.Leu60=)	rs1555201367
NM_000075.4(CDK4):c.218+35A>T

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