ClinVar Miner

Submissions for variant NG_009018.1(NF1):g.[134769_136954del2186;136931_139830del2900]

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
UAB Medical Genomics Laboratory, UAB Medicine RCV000258481 SCV000328423 pathogenic Neurofibromatosis, type 1 2013-09-30 no assertion criteria provided clinical testing

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