ClinVar Miner

Submissions for variant NM_002529.4(NTRK1):c.435G>C (p.Leu145=)

dbSNP: rs1647275742
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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 RCV001279996 SCV004644732 likely benign Hereditary insensitivity to pain with anhidrosis 2023-07-16 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279996 SCV001467138 uncertain significance Hereditary insensitivity to pain with anhidrosis 2020-04-17 no assertion criteria provided clinical testing

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