Variant (rsID / SNP)

rs111033618

rs111033618 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL2RG. Clinical significance in the table: Pathogenic.

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Reference-table entries

IL2RGPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Cytoband: Xq13.1
HGVS: NM_000206.3(IL2RG):c.664C>T (p.Arg222Cys)
Allele change: Missense_R222C

Associated conditions / phenotypes

Combined immunodeficiency, X-linked|Inborn genetic diseases|X-linked severe combined immunodeficiency

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.