List of variants in gene CDKN1C reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001122630.2(CDKN1C):c.-11+60G>A	rs143992355	0.02792
NM_001122630.2(CDKN1C):c.787+142C>T	rs534934487	0.00417
NM_001122630.2(CDKN1C):c.-132G>A	rs147317732	0.00329
NM_001122630.2(CDKN1C):c.636C>T (p.Ser212=)	rs540923047	0.00143
NM_001122630.2(CDKN1C):c.534T>C (p.Ala178=)	rs112196492	0.00004
NM_001122630.2(CDKN1C):c.504CCCGGC[2] (p.168AP[7])	rs878853629
NM_001122630.2(CDKN1C):c.567_578del (p.186_187AP[8])	rs878853634
NM_001122630.2(CDKN1C):c.573GGCCCC[2] (p.186AP[8])	rs759134767

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