ClinVar Miner

Submissions for variant NM_030973.4(MED25):c.1317-8G>T

dbSNP: rs1036590547
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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 RCV000527907 SCV000657758 likely benign Charcot-Marie-Tooth disease type 2 2017-07-31 criteria provided, single submitter clinical testing

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