List of variants in gene CDKN2A reported as benign by Invitae

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_058195.4(CDKN2A):c.193+9477T>G	rs3731217	0.12347
NM_000077.5(CDKN2A):c.442G>A (p.Ala148Thr)	rs3731249	0.02007
NM_000077.5(CDKN2A):c.379G>T (p.Ala127Ser)	rs6413464	0.00527
NM_000077.5(CDKN2A):c.174A>C (p.Arg58=)	rs201208890	0.00273
NM_000077.5(CDKN2A):c.430C>T (p.Arg144Cys)	rs116150891	0.00248
NM_000077.5(CDKN2A):c.150+37G>C	rs45456595	0.00212
NM_000077.5(CDKN2A):c.273G>A (p.Leu91=)	rs4987127	0.00045
NM_000077.5(CDKN2A):c.51C>A (p.Ala17=)	rs764362225	0.00019
NM_000077.5(CDKN2A):c.151-14G>A	rs767030551	0.00016
NM_000077.5(CDKN2A):c.405G>A (p.Gly135=)	rs751586391	0.00004
NM_000077.5(CDKN2A):c.151-4G>C	rs529380972	0.00001
NM_000077.5(CDKN2A):c.361C>T (p.Leu121=)	rs142371511
NM_000077.5(CDKN2A):c.369T>A (p.His123Gln)	rs6413463
NM_000077.5(CDKN2A):c.83T>G (p.Val28Gly)	rs775176191

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