ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.7870-20A>G

dbSNP: rs574898272
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Human Genetics, Inc, Center for Human Genetics, Inc RCV000660123 SCV000782113 uncertain significance Neurofibromatosis, type 1 2016-11-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000660123 SCV002407235 benign Neurofibromatosis, type 1 2024-12-31 criteria provided, single submitter clinical testing

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