ClinVar Miner

Submissions for variant NM_015271.5(TRIM2):c.870C>T (p.Asn290=) (rs35333794)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000535069 SCV000654630 benign Charcot-Marie-Tooth disease, axonal, type 2R 2019-12-31 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000535069 SCV001156817 benign Charcot-Marie-Tooth disease, axonal, type 2R 2019-03-13 criteria provided, single submitter clinical testing

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