ClinVar Miner

Submissions for variant NM_015271.5(TRIM2):c.454-13G>C

dbSNP: rs754383694
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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 RCV002207628 SCV002362557 likely benign Charcot-Marie-Tooth disease type 2R 2022-10-13 criteria provided, single submitter clinical testing

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