ClinVar Miner

Submissions for variant NM_002529.4(NTRK1):c.359+5G>T

dbSNP: rs1571685765
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Inherited Neuropathy Consortium RCV000790138 SCV000929529 uncertain significance Charcot-Marie-Tooth disease no assertion criteria provided literature only
Clinical Genetics, Academic Medical Center RCV001701318 SCV001925668 pathogenic not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001701318 SCV001956437 likely pathogenic not provided no assertion criteria provided clinical testing

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