ClinVar Miner

Submissions for variant NM_003331.5(TYK2):c.1011+11C>T

gnomAD frequency: 0.00006  dbSNP: rs370938717
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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 RCV001897835 SCV002147809 likely benign Immunodeficiency 35 2024-12-02 criteria provided, single submitter clinical testing

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