ClinVar Miner

Submissions for variant NM_000732.6(CD3D):c.275-18T>C

gnomAD frequency: 0.00005  dbSNP: rs200238286
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 RCV001522072 SCV001731539 benign Immunodeficiency 19 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001655784 SCV001869115 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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