ClinVar Miner

Submissions for variant NM_000022.4(ADA):c.407del (p.Gly136fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003475691 SCV004213556 likely pathogenic Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency 2023-02-27 criteria provided, single submitter clinical testing

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