ClinVar Miner

Submissions for variant NM_003331.5(TYK2):c.2430C>T (p.Asp810=)

gnomAD frequency: 0.00004  dbSNP: rs776363968
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 RCV002219176 SCV002377124 likely benign Immunodeficiency 35 2024-09-09 criteria provided, single submitter clinical testing

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