ClinVar Miner

Submissions for variant NM_020732.3(ARID1B):c.6357del (p.Asp2121fs) (rs1057519002)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Molecular Genetics,CHU RENNES RCV000414865 SCV000493095 likely pathogenic intellectual deficiency; dysmorphy no assertion criteria provided clinical testing

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