ClinVar Miner

Submissions for variant NM_003331.5(TYK2):c.1669+16dup

dbSNP: rs755109900
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002082554 SCV002322650 benign Immunodeficiency 35 2023-09-27 criteria provided, single submitter clinical testing

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