ClinVar Miner

Submissions for variant NM_015335.5(MED13L):c.73-1G>A

dbSNP: rs1555225472
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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 RCV000656295 SCV000778264 pathogenic not provided 2017-06-08 no assertion criteria provided clinical testing

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