ClinVar Miner

Submissions for variant NM_002529.3(NTRK1):c.851-33T>A (rs80356674)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000190819 SCV000244260 pathogenic Inborn genetic diseases 2014-01-21 criteria provided, single submitter clinical testing
GeneReviews RCV000020471 SCV000040904 pathologic Hereditary insensitivity to pain with anhidrosis 2008-08-05 no assertion criteria provided curation Converted during submission to Pathogenic.

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