List of variants in gene CDKN2A reported as benign by GeneDx

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000077.5(CDKN2A):c.*29G>C	rs11515	0.85710
NM_058195.4(CDKN2A):c.194-3810G>A	rs3814960	0.49402
NM_000077.5(CDKN2A):c.150+459T>C	rs3731239	0.25729
NM_058195.4(CDKN2A):c.193+174A>G	rs2811711	0.13731
NM_000077.5(CDKN2A):c.*69C>T	rs3088440	0.13094
NM_000077.5(CDKN2A):c.151-782G>C	rs3731246	0.11404
NM_000077.5(CDKN2A):c.442G>A (p.Ala148Thr)	rs3731249	0.02007
NM_000077.5(CDKN2A):c.*373C>G	rs3731255	0.01721
NM_000077.5(CDKN2A):c.379G>T (p.Ala127Ser)	rs6413464	0.00527
NM_000077.5(CDKN2A):c.458-471G>T	rs34011899	0.00517
NM_000077.5(CDKN2A):c.430C>T (p.Arg144Cys)	rs116150891	0.00248
NM_058195.4(CDKN2A):c.69C>T (p.Phe23=)	rs374360796	0.00024
NM_000077.5(CDKN2A):c.151-14G>A	rs767030551	0.00016
NM_000077.5(CDKN2A):c.384G>A (p.Arg128=)	rs199901898	0.00016
NM_000077.5(CDKN2A):c.459C>T (p.Asp153=)	rs778871932	0.00002
NM_000077.5(CDKN2A):c.150+6T>C	rs1025333664	0.00001
NM_000077.5(CDKN2A):c.151-4G>C	rs529380972	0.00001
NM_000077.5(CDKN2A):c.*223G>T	rs181996487
NM_000077.5(CDKN2A):c.150+1255C>A	rs2811708

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