List of variants in gene CDKN2A reported as uncertain significance for CDKN2A-related disorder

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000077.5(CDKN2A):c.150+1104C>A	rs756102261	0.00069
NM_000077.5(CDKN2A):c.365G>T (p.Gly122Val)	rs373291490	0.00016
NM_058195.4(CDKN2A):c.160C>A (p.Arg54Ser)	rs896054565	0.00006
NM_058195.4(CDKN2A):c.-9G>A	rs775302601	0.00004
NM_000077.5(CDKN2A):c.458-514A>G	rs1210653597	0.00001
NM_000077.5(CDKN2A):c.125A>G (p.Asn42Ser)	rs1060501264
NM_000077.5(CDKN2A):c.151-1104C>G	rs1819804753
NM_000077.5(CDKN2A):c.170C>T (p.Ala57Val)	rs372266620
NM_000077.5(CDKN2A):c.458-493G>C
NM_058195.4(CDKN2A):c.97dup (p.Glu33fs)	rs779306249

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