List of variants in gene CDKN2A reported by Breakthrough Genomics, Breakthrough Genomics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000077.5(CDKN2A):c.*29G>C	rs11515	0.86107
NM_058195.4(CDKN2A):c.194-3810G>A	rs3814960	0.49402
NM_058195.4(CDKN2A):c.193+174A>G	rs2811711	0.13194
NM_000077.5(CDKN2A):c.*69C>T	rs3088440	0.13094
NM_000077.5(CDKN2A):c.442G>A (p.Ala148Thr)	rs3731249	0.02007
NM_000077.5(CDKN2A):c.*373C>G	rs3731255	0.01721
NM_000077.5(CDKN2A):c.150+365T>G	rs115521447	0.01050
NM_000077.5(CDKN2A):c.458-471G>T	rs34011899	0.00517
NM_000077.5(CDKN2A):c.379G>T (p.Ala127Ser)	rs6413464	0.00490
NM_000077.5(CDKN2A):c.151-223G>A	rs138233963	0.00370
NM_000077.5(CDKN2A):c.174A>C (p.Arg58=)	rs201208890	0.00273
NM_000077.5(CDKN2A):c.150+216A>G	rs147602781	0.00257
NM_000077.5(CDKN2A):c.150+280C>T	rs150201743	0.00055

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