ClinVar Miner

Submissions for variant NM_002529.4(NTRK1):c.1650C>T (p.Ser550=)

gnomAD frequency: 0.00001  dbSNP: rs774664479
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
Invitae RCV001280009 SCV001595652 likely benign Hereditary insensitivity to pain with anhidrosis 2021-12-12 criteria provided, single submitter clinical testing
Natera, Inc. RCV001280009 SCV001467153 uncertain significance Hereditary insensitivity to pain with anhidrosis 2020-04-17 no assertion criteria provided clinical testing

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