ClinVar Miner

Submissions for variant NM_003327.4(TNFRSF4):c.198G>T (p.Pro66=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002611138 SCV003500215 likely benign Combined immunodeficiency due to OX40 deficiency 2024-01-16 criteria provided, single submitter clinical testing

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