C1969893[trait identifier] AND "Center for Genomic Medicine, King Fais - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3064403	NM_173602.3(DIP2B):c.1034G>A (p.Arg345His)	DIP2B (R345H)	Single nucleotide variant (missense variant)	Intellectual disability, FRA12A type	GUncertain significance
Select item 3064489	NM_173602.3(DIP2B):c.4044-23_4044-15del	DIP2B	Deletion (intron variant)	Intellectual disability, FRA12A type	GLikely pathogenic