Variant (rsID / SNP)

rs12722608

rs12722608 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL2RA. Location: chromosome 10, position 6,052,841. Clinical significance in the table: Benign.

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Reference-table entries

IL2RABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:6052841
Cytoband: 10p15.1
HGVS: NM_000417.3(IL2RA):c.*1994G>T
Allele change: Silent

Associated conditions / phenotypes

Immunodeficiency due to CD25 deficiency

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.