ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.7970+2T>G

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV004018250 SCV004848925 likely pathogenic Neurofibromatosis, type 1 2023-02-02 criteria provided, single submitter clinical testing The c.7970+2T>G variant in NF1 has not been reported in individuals with neurofibromatosis as absent from large population databases. This variant occurs within the canonical splice site (+/- 1,2) and is predicted to cause altered splicing leading to an abnormal or absent protein.Loss of function of the NF1 gene is an established disease mechanism in autosomal dominant neurofibromatosis. In summary, though additional studies are required to fully establish its clinical significance, this variant meets criteria to be classified as likely pathogenic for autosomal dominant neurofibromatosis.ACMG/AMP criteria applied: PVS1_Strong, PM2_Supporting.

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