C1832950[trait identifier] AND "OMIM"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 224962	NM_170675.5(MEIS2):c.992GAA[2] (p.Arg333del)	MEIS2 (R320del +2 more)	Microsatellite (inframe_deletion +1 more)	Inborn genetic diseases +2 more	GPathogenic/Likely pathogenic
Select item 803063	NM_170675.5(MEIS2):c.934_937del (p.Leu312fs)	MEIS2 (L224fs +2 more)	Deletion (frameshift variant)	Cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies +1 more	GPathogenic/Likely pathogenic
Select item 418712	NM_170675.5(MEIS2):c.905C>T (p.Pro302Leu)	MEIS2 (P289L +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 1527861	NM_170675.5(MEIS2):c.639+1G>A	MEIS2	Single nucleotide variant (splice donor variant)	Cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies	GPathogenic
Select item 427215	NM_170675.5(MEIS2):c.611C>G (p.Ser204Ter)	MEIS2 (S204* +2 more)	Single nucleotide variant (nonsense +1 more)	Cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies	GPathogenic
Select item 427214	NG_029108.1:g.120078_181902dup	MEIS2	Duplication	Cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies	GPathogenic

ClinVar