List of variants in gene CDKN2A reported as uncertain significance by Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden

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.458-491C>T	rs181044510	0.00229
NM_000077.5(CDKN2A):c.150+37G>C	rs45456595	0.00212
NM_000077.5(CDKN2A):c.150+196G>A	rs2131109431
NM_000077.5(CDKN2A):c.170C>T (p.Ala57Val)	rs372266620
NM_000077.5(CDKN2A):c.80A>C (p.Glu27Ala)	rs1554656403

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