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

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004064.5(CDKN1B):c.206C>T (p.Pro69Leu)	rs777354267	0.00002
NM_004064.5(CDKN1B):c.174dup (p.Lys59fs)
NM_004064.5(CDKN1B):c.229C>T (p.Gln77Ter)

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