ClinVar Miner

Submissions for variant NM_001007792.1(NTRK1):c.1698-4del (rs1799770)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000712457 SCV000842955 benign not provided 2018-01-12 criteria provided, single submitter clinical testing
GeneDx RCV000616650 SCV000729338 benign not specified 2018-03-08 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Illumina Clinical Services Laboratory,Illumina RCV000328341 SCV000349057 likely benign Hereditary insensitivity to pain with anhidrosis 2016-06-14 criteria provided, single submitter clinical testing

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