ClinVar Miner

Submissions for variant NM_015271.5(TRIM2):c.2142C>T (p.Asp714=)

dbSNP: rs2149583773
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002144459 SCV002469461 likely benign Charcot-Marie-Tooth disease type 2R 2021-11-19 criteria provided, single submitter clinical testing

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