ClinVar Miner

Submissions for variant NM_000215.4(JAK3):c.*222CT[1]

dbSNP: rs3212801
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV001731605 SCV000411092 benign Severe combined immunodeficiency disease 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001594961 SCV001828992 benign not provided 2018-07-09 criteria provided, single submitter clinical testing

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