ClinVar Miner

Submissions for variant NM_000142.5(FGFR3):c.1266+25C>T

gnomAD frequency: 0.00088  dbSNP: rs200827273
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Faculté Pluridciplinaire Nador, Université Mohamed Premier RCV001250967 SCV001250950 uncertain significance Squamous cell lung carcinoma 2020-05-05 no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001724247 SCV001951984 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001724247 SCV001970019 likely benign not provided no assertion criteria provided clinical testing

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