ClinVar Miner

Submissions for variant NM_181882.3(PRX):c.382-17C>T

dbSNP: rs889158287
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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 RCV002219224 SCV002377149 likely benign Charcot-Marie-Tooth disease type 4 2022-08-18 criteria provided, single submitter clinical testing

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