ClinVar Miner

Submissions for variant NM_002529.4(NTRK1):c.1805+8C>A

gnomAD frequency: 0.00002  dbSNP: rs780424308
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000938935 SCV001084765 likely benign Hereditary insensitivity to pain with anhidrosis 2023-12-17 criteria provided, single submitter clinical testing
Natera, Inc. RCV000938935 SCV001463406 uncertain significance Hereditary insensitivity to pain with anhidrosis 2020-01-24 no assertion criteria provided clinical testing

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