ClinVar Miner

Submissions for variant NM_000267.3(NF1):c.288+230_480-1812delins323

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Medical Genomics Laboratory, Department of Genetics UAB RCV000200945 SCV000255519 pathogenic Neurofibromatosis, type 1 no assertion criteria provided clinical testing

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