ClinVar Miner

Submissions for variant NM_002506.3(NGF):c.441C>T (p.Thr147=)

dbSNP: rs765111580
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002164261 SCV002478079 likely benign Congenital sensory neuropathy with selective loss of small myelinated fibers 2024-09-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004711885 SCV005259313 likely benign not provided criteria provided, single submitter not provided

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