ClinVar Miner

Submissions for variant NM_016156.6(MTMR2):c.1387-8T>C

dbSNP: rs2496436883
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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 RCV003581176 SCV004280907 likely benign Charcot-Marie-Tooth disease type 4 2023-04-09 criteria provided, single submitter clinical testing

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