ClinVar Miner

Submissions for variant NM_002529.4(NTRK1):c.303T>A (p.Ser101Arg)

dbSNP: rs2102886126
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Molecular Genetics (Pr. Bezieau's lab), CHU de Nantes RCV001780051 SCV002016303 likely pathogenic Neurodevelopmental disorder 2021-09-13 criteria provided, single submitter clinical testing

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