Variants in gene CDKN1B with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 16

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HGVS	dbSNP	gnomAD frequency
NM_004064.5(CDKN1B):c.426G>A (p.Thr142=)	rs149775942	0.00366
NM_004064.5(CDKN1B):c.577C>T (p.Leu193Phe)	rs73281150	0.00338
NM_004064.5(CDKN1B):c.543C>G (p.Ala181=)	rs140177202	0.00064
NM_004064.5(CDKN1B):c.356T>C (p.Ile119Thr)	rs142833529	0.00057
NM_004064.5(CDKN1B):c.518A>G (p.Asn173Ser)	rs141509450	0.00042
NM_004064.5(CDKN1B):c.155T>G (p.Met52Arg)	rs543122580	0.00037
NM_004064.5(CDKN1B):c.114C>T (p.His38=)	rs141178987	0.00031
NM_004064.5(CDKN1B):c.476-5C>T	rs370509436	0.00031
NM_004064.5(CDKN1B):c.407A>G (p.Asp136Gly)	rs546234840	0.00020
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.234G>A (p.Glu78=)	rs751794433	0.00007
NM_004064.5(CDKN1B):c.475+5T>C	rs781394293	0.00001
NM_004064.5(CDKN1B):c.277C>T (p.Arg93Trp)	rs140167393
NM_004064.5(CDKN1B):c.283C>G (p.Pro95Ala)	rs188579132
NM_004064.5(CDKN1B):c.397C>A (p.Pro133Thr)	rs137985549

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