ClinVar Miner

Submissions for variant NM_003331.5(TYK2):c.753C>T (p.Ser251=)

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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 RCV002880233 SCV003229821 likely benign Immunodeficiency 35 2023-08-17 criteria provided, single submitter clinical testing

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