ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.*859AT[7]

dbSNP: rs369548314
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000291178 SCV000401841 benign Neurofibromatosis, type 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000343788 SCV000401842 benign Café-au-lait macules with pulmonary stenosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000381987 SCV000401843 benign Neurofibromatosis-Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000285167 SCV000401844 benign Neurofibromatosis, familial spinal 2016-06-14 criteria provided, single submitter clinical testing

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