"Ambry Genetics"[submitter] AND "RAC3"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3150974	NM_005052.3(RAC3):c.292T>C (p.Tyr98His)	RAC3 (Y98H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2233801	NM_005052.3(RAC3):c.413C>T (p.Thr138Ile)	RAC3 (T138I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2612224	NM_005052.3(RAC3):c.449-5G>A	RAC3	Single nucleotide variant (intron variant)	Inborn genetic diseases	GLikely benign

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