List of variants in gene CDKN1B reported as benign for not provided

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_004064.5(CDKN1B):c.-79T>C	rs34330	0.69820
NM_004064.5(CDKN1B):c.*9-222T>C	rs34327	0.49862
NM_004064.5(CDKN1B):c.326T>G (p.Val109Gly)	rs2066827	0.36014
NM_004064.5(CDKN1B):c.-266C>G	rs3093728	0.00372
NM_004064.5(CDKN1B):c.518A>G (p.Asn173Ser)	rs141509450	0.00042
NM_004064.5(CDKN1B):c.373T>A (p.Ser125Thr)	rs765681672	0.00017
NM_004064.5(CDKN1B):c.54C>T (p.Ala18=)	rs151027466	0.00009
NM_004064.5(CDKN1B):c.225G>C (p.Glu75Asp)	rs139727620	0.00006
NM_004064.5(CDKN1B):c.258G>A (p.Glu86=)	rs142940486	0.00006
NM_004064.5(CDKN1B):c.246C>T (p.Gly82=)	rs376624980	0.00003
NM_004064.5(CDKN1B):c.282C>T (p.Pro94=)	rs751288223	0.00001
NM_004064.5(CDKN1B):c.-7G>A	rs751341214

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