ClinVar Miner

Submissions for variant NM_003331.5(TYK2):c.3028-4C>T

gnomAD frequency: 0.00003  dbSNP: rs755053371
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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 RCV002109802 SCV002398148 likely benign Immunodeficiency 35 2022-10-24 criteria provided, single submitter clinical testing

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