List of variants in gene CDKN1C reported as uncertain significance for IMAGe syndrome

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001122630.2(CDKN1C):c.-11+61G>A	rs188494894	0.00603
NM_001122630.2(CDKN1C):c.853C>T (p.Pro285Ser)	rs531059713	0.00007
NM_001122630.2(CDKN1C):c.316C>T (p.Pro106Ser)	rs570636789	0.00004
NM_001122630.2(CDKN1C):c.*5+1G>A
NM_001122630.2(CDKN1C):c.820G>A (p.Glu274Lys)

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