ClinVar Miner

List of variants in gene CDKN2A reported as uncertain significance by True Health Diagnostics

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000077.5(CDKN2A):c.197A>G (p.His66Arg)	rs756750256	0.00009
NM_000077.5(CDKN2A):c.425A>G (p.His142Arg)	rs759922342	0.00001

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