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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000206.3(IL2RG):c.406C>T (p.Arg136Trp) | Likely Benign | T-B+ severe combined immunodeficiency due to gamma chain deficiency | 2024-06-13 | 1.0 | ClinGen Severe Combined Immunodeficiency Disease Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for IL2RG Version 1.0.0 | IL2RG |
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