ClinVar Miner

Submissions for variant NM_002529.4(NTRK1):c.2301G>A (p.Glu767=)

dbSNP: rs753397054
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001277510 SCV001668368 likely benign Hereditary insensitivity to pain with anhidrosis 2021-11-27 criteria provided, single submitter clinical testing
Natera, Inc. RCV001277510 SCV001464469 uncertain significance Hereditary insensitivity to pain with anhidrosis 2020-04-18 no assertion criteria provided clinical testing

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