List of variants in gene CDKN2A reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000077.5(CDKN2A):c.318G>A (p.Val106=)	rs199888003	0.00026
NM_000077.5(CDKN2A):c.261G>A (p.Arg87=)	rs546300971	0.00010
NM_000077.5(CDKN2A):c.87G>A (p.Arg29=)	rs540871544	0.00009
NM_000077.5(CDKN2A):c.197A>G (p.His66Arg)	rs756750256	0.00004
NM_000077.5(CDKN2A):c.147C>A (p.Ile49=)	rs200738474	0.00003
NM_000077.5(CDKN2A):c.258C>T (p.Ala86=)	rs1001405220	0.00001
NM_000077.5(CDKN2A):c.402G>T (p.Ala134=)	rs878853649	0.00001
NM_000077.5(CDKN2A):c.177G>A (p.Val59=)	rs527503775
NM_000077.5(CDKN2A):c.213C>T (p.Asn71=)	rs2131095688
NM_000077.5(CDKN2A):c.370C>T (p.Arg124Cys)	rs34170727
NM_000077.5(CDKN2A):c.441C>A (p.Ala147=)	rs1057524065
NM_000077.5(CDKN2A):c.84G>A (p.Val28=)	rs1461154048

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