ClinVar Miner

Submissions for variant NM_002585.4(PBX1):c.838-1G>C

dbSNP: rs1669636373
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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 (Pr. Bezieau's lab), CHU de Nantes RCV001171616 SCV001334414 likely pathogenic not provided 2019-11-06 criteria provided, single submitter clinical testing

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