ClinVar Miner

Submissions for variant NM_002529.3(NTRK1):c.1887C>T (p.Ala629=) (rs6337)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000287221 SCV000349062 benign Hereditary insensitivity to pain with anhidrosis 2016-06-14 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000516727 SCV000614366 benign not specified 2017-07-28 criteria provided, single submitter clinical testing
Inherited Neuropathy Consortium RCV000516727 SCV000928972 uncertain significance not specified no assertion criteria provided literature only

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