List of variants in gene CDKN2A reported as benign for not specified

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_000077.5(CDKN2A):c.*69C>T	rs3088440	0.13094
NM_000077.5(CDKN2A):c.442G>A (p.Ala148Thr)	rs3731249	0.02007
NM_000077.5(CDKN2A):c.150+214del	rs200129494	0.01057
NM_000077.5(CDKN2A):c.379G>T (p.Ala127Ser)	rs6413464	0.00527
NM_000077.5(CDKN2A):c.151-1238G>A	rs3731245	0.00519
NM_000077.5(CDKN2A):c.430C>T (p.Arg144Cys)	rs116150891	0.00248
NM_000077.5(CDKN2A):c.273G>A (p.Leu91=)	rs4987127	0.00045
NM_000077.5(CDKN2A):c.298G>T (p.Ala100Ser)	rs200863613	0.00038
NM_000077.5(CDKN2A):c.318G>A (p.Val106=)	rs199888003	0.00026
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.197A>G (p.His66Arg)	rs756750256	0.00004
NM_000077.5(CDKN2A):c.405G>A (p.Gly135=)	rs751586391	0.00004
NM_000077.5(CDKN2A):c.*6C>G	rs375628411	0.00002
NM_000077.5(CDKN2A):c.151-4G>C	rs529380972	0.00001
NM_000077.5(CDKN2A):c.150+1255C>A	rs2811708
NM_000077.5(CDKN2A):c.369T>A (p.His123Gln)	rs6413463

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