"RAC3-related disorder"[Disease/phenotype] AND "PreventionGenetics, pa - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3025052	NM_005052.3(RAC3):c.72G>A (p.Thr24=)	RAC3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2628836	NM_005052.3(RAC3):c.94T>C (p.Tyr32His)	RAC3 (Y32H)	Single nucleotide variant (missense variant)	RAC3-related disorder	GUncertain significance
Select item 3034130	NM_005052.3(RAC3):c.235C>T (p.Leu79=)	RAC3	Single nucleotide variant (synonymous variant)	RAC3-related disorder	GLikely benign
Select item 3051136	NM_005052.3(RAC3):c.306G>A (p.Arg102=)	RAC3	Single nucleotide variant (synonymous variant)	RAC3-related disorder	GLikely benign
Select item 3056579	NM_005052.3(RAC3):c.477C>T (p.Ala159=)	RAC3 (P161S)	Single nucleotide variant (missense variant +1 more)	RAC3-related disorder	GBenign
Select item 3034656	NM_005052.3(RAC3):c.522C>T (p.Arg174=)	RAC3	Single nucleotide variant (3 prime UTR variant +1 more)	RAC3-related disorder	GLikely benign
Select item 2648480	NM_005052.3(RAC3):c.575T>C (p.Phe192Ser)	RAC3 (F192S)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 3046318	NM_005052.3(RAC3):c.*3C>G	RAC3	Single nucleotide variant (3 prime UTR variant)	RAC3-related disorder	GLikely benign

ClinVar