ClinVar Miner

Submissions for variant NM_003331.5(TYK2):c.2311+16G>C

dbSNP: rs12720300
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001522724 SCV001732317 benign Immunodeficiency 35 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001535232 SCV001752227 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001535232 SCV005311955 benign not provided criteria provided, single submitter not provided

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