List of variants in gene CDKN2A reported as likely benign by Quest Diagnostics Nichols Institute San Juan Capistrano

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000077.5(CDKN2A):c.365G>T (p.Gly122Val)	rs373291490	0.00016
NM_000077.5(CDKN2A):c.87G>A (p.Arg29=)	rs540871544	0.00009
NM_000077.5(CDKN2A):c.225C>G (p.Pro75=)	rs762397298	0.00001
NM_000077.5(CDKN2A):c.468T>C (p.Asp156=)	rs749753811	0.00001
NM_000077.5(CDKN2A):c.225C>T (p.Pro75=)	rs762397298
NM_000077.5(CDKN2A):c.288G>A (p.Val96=)	rs557319056
NM_000077.5(CDKN2A):c.369T>A (p.His123Gln)	rs6413463
NM_000077.5(CDKN2A):c.369T>C (p.His123=)	rs6413463

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