List of variants in gene CDKN2A reported as benign for Hereditary cancer-predisposing syndrome

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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.442G>A (p.Ala148Thr)	rs3731249	0.02007
NM_000077.5(CDKN2A):c.379G>T (p.Ala127Ser)	rs6413464	0.00490
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.151-4G>C	rs529380972	0.00055
NM_000077.5(CDKN2A):c.298G>T (p.Ala100Ser)	rs200863613	0.00035
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.69T>G (p.Gly23=)	rs766772030	0.00010
NM_000077.5(CDKN2A):c.*6C>G	rs375628411	0.00002
NM_000077.5(CDKN2A):c.122C>A (p.Pro41Gln)	rs373407950	0.00002
NM_000077.5(CDKN2A):c.369T>A (p.His123Gln)	rs6413463

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