ClinVar Miner

Submissions for variant NM_003331.5(TYK2):c.318-17G>A

gnomAD frequency: 0.00017  dbSNP: rs201764291
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002183314 SCV002429273 benign Immunodeficiency 35 2024-01-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004717882 SCV005311986 benign not provided criteria provided, single submitter not provided

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