ClinVar Miner

Submissions for variant NM_002139.4(RBMX):c.217-2dup

Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003135217 SCV003813793 uncertain significance Syndromic X-linked intellectual disability Shashi type 2021-07-01 criteria provided, single submitter clinical testing

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