C4540321[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 218339	NM_000965.5(RARB):c.638T>C (p.Leu213Pro)	RARB (L213P +4 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GPathogenic/Likely pathogenic
Select item 88762	NM_000965.5(RARB):c.1159C>T (p.Arg387Cys)	RARB (R387C +5 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability, autosomal dominant 48 +3 more	GPathogenic/Likely pathogenic
Select item 1027690	NM_006908.5(RAC1):c.168G>C (p.Trp56Cys)	RAC1 (W56C)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 48	GLikely pathogenic
Select item 974895	NM_006908.5(RAC1):c.198A>T (p.Arg66Ser)	RAC1 (R66S)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 48 +1 more	GConflicting classifications of pathogenicity
Select item 1033910	NM_006908.5(RAC1):c.372C>G (p.Asp124Glu)	RAC1 (D124E +1 more)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 48	GUncertain significance
Select item 625787	GRCh37/hg19 7p22.1(chr7:6385256-6431775)	RAC1, FAM220A	Copy number loss	Intellectual disability, autosomal dominant 48	GPathogenic

ClinVar