ClinVar Miner

Submissions for variant NM_001007792.1(NTRK1):c.986A>G (p.Tyr329Cys) (rs121964869)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000013104 SCV000033351 pathogenic Hereditary insensitivity to pain with anhidrosis 2002-08-01 no assertion criteria provided literature only
Inherited Neuropathy Consortium RCV000789504 SCV000928860 uncertain significance Charcot-Marie-Tooth disease no assertion criteria provided literature only

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