Variants in gene CDKN1C with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001122630.2(CDKN1C):c.-11+60G>A	rs143992355	0.02792
NM_001122630.2(CDKN1C):c.495G>C (p.Ala165=)	rs533485167	0.01351
NM_001122630.2(CDKN1C):c.99C>T (p.Arg33=)	rs149717696	0.00208
NM_001122630.2(CDKN1C):c.675G>A (p.Glu225=)	rs3741341	0.00183
NM_001122630.2(CDKN1C):c.636C>T (p.Ser212=)	rs540923047	0.00143
NM_001122630.2(CDKN1C):c.702G>A (p.Gly234=)	rs556682082	0.00065
NM_001122630.2(CDKN1C):c.455CTCCGGTCGCGG[2] (p.152APVA[2])	rs565544512
NM_001122630.2(CDKN1C):c.567_572del (p.186_187AP[9])	rs1060503860
NM_001122630.2(CDKN1C):c.567_578del (p.186_187AP[8])	rs878853634
NM_001122630.2(CDKN1C):c.567_578dup (p.186_187AP[12])	rs878853634
NM_001122630.2(CDKN1C):c.567_584del (p.186_187AP[7])	rs878853636
NM_001122630.2(CDKN1C):c.567_590del (p.186_187AP[6])	rs878853637
NM_001122630.2(CDKN1C):c.573GGCCCC[2] (p.186AP[8])	rs759134767
NM_001122630.2(CDKN1C):c.573GGCCCC[3] (p.186AP[9])	rs759134767

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