ClinVar Miner

Submissions for variant NM_001770.6(CD19):c.*129GT[14]

dbSNP: rs10633752
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 RCV000403832 SCV000396439 uncertain significance Common Variable Immune Deficiency, Recessive 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001690061 SCV001906580 benign not provided 2021-06-19 criteria provided, single submitter clinical testing

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