List of variants reported as pathogenic for combined immunodeficiency, X-linked

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000206.3(IL2RG):c.202G>A (p.Glu68Lys)	rs1057520644
NM_000206.3(IL2RG):c.664C>T (p.Arg222Cys)	rs111033618
NM_000206.3(IL2RG):c.670C>T (p.Arg224Trp)	rs869320658
NM_000206.3(IL2RG):c.676C>T (p.Arg226Cys)	rs869320659
NM_000206.3(IL2RG):c.878T>A (p.Leu293Gln)	rs137852510
NM_000206.3(IL2RG):c.924G>C (p.Ser308=)
NM_000206.3(IL2RG):c.982C>T (p.Arg328Ter)	rs1064793347

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