ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.*871del

gnomAD frequency: 0.01312  dbSNP: rs759306393
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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 RCV000342532 SCV000401845 uncertain significance Neurofibromatosis-Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000403226 SCV000401846 uncertain significance Neurofibromatosis, familial spinal 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000302806 SCV000401847 uncertain significance Café-au-lait macules with pulmonary stenosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000337101 SCV000401848 uncertain significance Neurofibromatosis, type 1 2016-06-14 criteria provided, single submitter clinical testing

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