List of variants in gene IL2RG reported as uncertain significance for Combined immunodeficiency, X-linked

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000206.3(IL2RG):c.1061A>G (p.His354Arg)	rs771221019	0.00002
NM_000206.3(IL2RG):c.318A>G (p.Leu106=)	rs1389116834
NM_000206.3(IL2RG):c.484C>G (p.Leu162Val)	rs2147749821

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