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

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000077.5(CDKN2A):c.150+216A>G	rs147602781	0.00277
NM_000077.5(CDKN2A):c.430C>T (p.Arg144Cys)	rs116150891	0.00248
NM_000077.5(CDKN2A):c.273G>A (p.Leu91=)	rs4987127	0.00045
NM_058195.4(CDKN2A):c.-28C>G	rs149253558	0.00035
NM_058195.4(CDKN2A):c.69C>T (p.Phe23=)	rs374360796	0.00024
NM_000077.5(CDKN2A):c.458-492G>C	rs527814073	0.00021
NM_000077.5(CDKN2A):c.151-14G>A	rs767030551	0.00016
NM_000077.5(CDKN2A):c.384G>A (p.Arg128=)	rs199901898	0.00016
NM_000077.5(CDKN2A):c.150+40C>T	rs1057517604	0.00003
NM_000077.5(CDKN2A):c.458-541A>G	rs938889880	0.00003
NM_000077.5(CDKN2A):c.150+20C>T	rs550846229	0.00002
NM_000077.5(CDKN2A):c.151-4G>C	rs529380972	0.00001
NM_058195.4(CDKN2A):c.193+7A>G	rs770519197	0.00001
NM_000077.5(CDKN2A):c.150+104_150+105del	rs1057517608
NM_000077.5(CDKN2A):c.150+1104C>T	rs756102261
NM_000077.5(CDKN2A):c.150+170dup	rs753316964
NM_000077.5(CDKN2A):c.150+193G>A	rs1057517587
NM_000077.5(CDKN2A):c.150+71_150+76del	rs753508262
NM_000077.5(CDKN2A):c.458-465G>C	rs563204204

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