ClinVar Miner

Submissions for variant NM_002529.4(NTRK1):c.1431C>T (p.Ser477=)

gnomAD frequency: 0.00003  dbSNP: rs532119440
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001504489 SCV001709369 likely benign Hereditary insensitivity to pain with anhidrosis 2023-08-29 criteria provided, single submitter clinical testing

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