C1832386[trait identifier] AND "OMIM"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 717	NM_001109809.5(ZFP57):c.1383del (p.Tyr462fs)	ZFP57 (Y390fs +1 more)	Deletion (frameshift variant)	Diabetes mellitus, transient neonatal, 1	GPathogenic
Select item 718	NM_001109809.5(ZFP57):c.1372C>G (p.His458Asp)	ZFP57 (H458D +1 more)	Single nucleotide variant (missense variant)	Diabetes mellitus, transient neonatal, 1	GPathogenic
Select item 721	NM_001109809.5(ZFP57):c.898_905del (p.Gly299_Thr300insTer)	ZFP57	Deletion (nonsense)	Diabetes mellitus, transient neonatal, 1	GPathogenic
Select item 720	NM_001109809.5(ZFP57):c.829C>A (p.His277Asn)	ZFP57 (H277N +1 more)	Single nucleotide variant (missense variant)	Diabetes mellitus, transient neonatal, 1	GPathogenic
Select item 715	NM_001109809.2(ZFP57):c.783C>A (p.Cys261Ter)	ZFP57 (C261* +1 more)	Single nucleotide variant (nonsense)	Diabetes mellitus, transient neonatal, 1	GPathogenic
Select item 719	NM_001109809.5(ZFP57):c.743G>A (p.Arg248His)	ZFP57 (R248H +1 more)	Single nucleotide variant (missense variant)	Diabetes mellitus, transient neonatal, 1	GPathogenic
Select item 716	NM_001109809.5(ZFP57):c.317_318del (p.Glu106fs)	ZFP57 (E34fs +1 more)	Microsatellite (frameshift variant)	Diabetes mellitus, transient neonatal, 1	GPathogenic

ClinVar