ClinVar Miner

Submissions for variant NM_003331.5(TYK2):c.861G>A (p.Glu287=)

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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 RCV005113049 SCV005729308 likely benign Immunodeficiency 35 2024-03-18 criteria provided, single submitter clinical testing

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