C2700553[trait identifier] AND "Victorian Clinical Genetics Services, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 36717	NM_000536.4(RAG2):c.1247G>T (p.Trp416Leu)	RAG2 (W416L)	Single nucleotide variant (missense variant)	Recombinase activating gene 2 deficiency	GLikely pathogenic FDA Recognized database
Select item 13135	NM_000536.4(RAG2):c.644C>T (p.Thr215Ile)	RAG2 (T215I)	Single nucleotide variant (missense variant)	Recombinase activating gene 2 deficiency	GBenign FDA Recognized database