ClinVar Miner

Submissions for variant NM_002529.4(NTRK1):c.1521C>T (p.Arg507=)

dbSNP: rs901135479
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001280006 SCV002930210 likely benign Hereditary insensitivity to pain with anhidrosis 2022-06-26 criteria provided, single submitter clinical testing
Natera, Inc. RCV001280006 SCV001467149 uncertain significance Hereditary insensitivity to pain with anhidrosis 2020-04-17 no assertion criteria provided clinical testing

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