ClinVar Miner

Submissions for variant NM_000192.3:c.(362+1_363-1)_(510+1_511-1)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille RCV000782332 SCV000920853 pathogenic Holt-Oram syndrome 2018-06-14 no assertion criteria provided clinical testing

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