ClinVar Miner

Submissions for variant NM_001007792.1(NTRK1):c.1908C>T (p.Ser636=) (rs757891009)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000932635 SCV001078319 likely benign not provided 2018-07-03 criteria provided, single submitter clinical testing
Invitae RCV001430555 SCV001633297 likely benign Hereditary insensitivity to pain with anhidrosis 2018-07-01 criteria provided, single submitter clinical testing

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