"Blueprint Genetics"[submitter] AND "IL2RG"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 636787	NM_000206.3(IL2RG):c.*306A>C	IL2RG	Single nucleotide variant (3 prime UTR variant)	not provided	GUncertain significance
Select item 532191	NM_000206.3(IL2RG):c.821T>C (p.Ile274Thr)	IL2RG (I274T)	Single nucleotide variant (missense variant)	X-linked severe combined immunodeficiency	GUncertain significance FDA Recognized database
Select item 636917	NM_000206.3(IL2RG):c.184T>A (p.Cys62Ser)	IL2RG (C62S)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic

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