List of variants in gene CDKN2A reported as uncertain significance by Revvity Omics, Revvity

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_000077.5(CDKN2A):c.325G>C (p.Ala109Pro)	rs372481694	0.00009
NM_000077.5(CDKN2A):c.239G>C (p.Arg80Pro)	rs1057519883	0.00001
NM_000077.5(CDKN2A):c.64C>T (p.Arg22Trp)	rs374921006

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