ClinVar Miner

Submissions for variant NM_002529.4(NTRK1):c.656delinsTT (p.Gly219fs)

dbSNP: rs2102894535
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Provincial Medical Genetics Program of British Columbia, University of British Columbia RCV002211040 SCV002496406 likely pathogenic Hereditary insensitivity to pain with anhidrosis 2022-01-01 criteria provided, single submitter clinical testing

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