ClinVar Miner

Submissions for variant NM_133433.4(NIPBL):c.5427+3A>G

dbSNP: rs1363419528
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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 RCV000656297 SCV000778266 uncertain significance not provided 2017-06-12 no assertion criteria provided clinical testing

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