Variants in gene CDKN1B with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004064.5(CDKN1B):c.518A>G (p.Asn173Ser)	rs141509450	0.00042
NM_004064.5(CDKN1B):c.-80C>T	rs551236750	0.00021
NM_004064.5(CDKN1B):c.407A>G (p.Asp136Gly)	rs546234840	0.00020
NM_004064.5(CDKN1B):c.482C>G (p.Ser161Cys)	rs373917399	0.00014
NM_004064.5(CDKN1B):c.281C>T (p.Pro94Leu)	rs757917082	0.00011
NM_004064.5(CDKN1B):c.125C>T (p.Thr42Ile)	rs200422211	0.00009
NM_004064.5(CDKN1B):c.54C>T (p.Ala18=)	rs151027466	0.00009
NM_004064.5(CDKN1B):c.-7G>A	rs751341214

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