ClinVar Miner

Submissions for variant NM_003331.5(TYK2):c.466-11C>T

dbSNP: rs2145259990
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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 RCV002081998 SCV002430533 likely benign Immunodeficiency 35 2021-11-22 criteria provided, single submitter clinical testing

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