List of variants in gene CDKN2A reported as likely benign by Mendelics

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000077.5(CDKN2A):c.150+37G>C	rs45456595	0.00212
NM_000077.5(CDKN2A):c.150+280C>T	rs150201743	0.00056
NM_000077.5(CDKN2A):c.457+83C>T	rs560686386	0.00038
NM_000077.5(CDKN2A):c.457+1129C>T	rs774962789	0.00019
NM_000077.5(CDKN2A):c.384G>A (p.Arg128=)	rs199901898	0.00016
NM_000077.5(CDKN2A):c.457+30C>T	rs780868128	0.00002
NM_000077.5(CDKN2A):c.151-66A>G	rs890179220	0.00001
NM_000077.5(CDKN2A):c.458-525G>T	rs1448745459	0.00001
NM_000077.5(CDKN2A):c.150+11G>A	rs1587339427
NM_000077.5(CDKN2A):c.150+137T>G	rs1587338978
NM_000077.5(CDKN2A):c.369T>A (p.His123Gln)	rs6413463
NM_000077.5(CDKN2A):c.369T>C (p.His123=)	rs6413463
NM_058195.4(CDKN2A):c.194-3834C>G	rs917599759
NM_058195.4(CDKN2A):c.194-3853_194-3852insGCG	rs1587341124
NM_058195.4(CDKN2A):c.194-3854_194-3853insGTG	rs1587341128

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