ClinVar Miner

Submissions for variant NM_001007792.1(NTRK1):c.484+9C>T (rs771749558)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000946394 SCV001092524 likely benign not provided 2018-05-12 criteria provided, single submitter clinical testing
Invitae RCV001443051 SCV001646011 likely benign Hereditary insensitivity to pain with anhidrosis 2020-09-30 criteria provided, single submitter clinical testing

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