"University of Washington Department of Laboratory Medicine, Universit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 224565	NM_000077.5(CDKN2A):c.457+929C>T	CDKN2A	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 9415	NM_000077.5(CDKN2A):c.71G>C (p.Arg24Pro)	CDKN2A (R24P)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +5 more	GPathogenic/Likely pathogenic
Select item 223663	NM_058195.4(CDKN2A):c.194-4112A>T	CDKN2A	Single nucleotide variant (intron variant)	not provided	GLikely benign

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ClinVar