List of variants in gene CDKN2A reported as likely benign by Myriad Genetics, Inc.

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000077.5(CDKN2A):c.430C>T (p.Arg144Cys)	rs116150891	0.00248
NM_000077.5(CDKN2A):c.151-4G>C	rs529380972	0.00055
NM_000077.5(CDKN2A):c.151-14G>A	rs767030551	0.00016
NM_058195.4(CDKN2A):c.193+7A>G	rs770519197	0.00001
NM_000077.5(CDKN2A):c.369T>A (p.His123Gln)	rs6413463

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