ClinVar Miner

Submissions for variant NM_002529.4(NTRK1):c.1177+4C>T

dbSNP: rs964771053
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Natera, Inc. RCV001280003 SCV001467146 uncertain significance Hereditary insensitivity to pain with anhidrosis 2020-08-14 no assertion criteria provided clinical testing

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