ClinVar Miner

Submissions for variant NM_181882.3(PRX):c.28-20C>T

dbSNP: rs757487813
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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 RCV002116857 SCV002384900 likely benign Charcot-Marie-Tooth disease type 4 2023-09-15 criteria provided, single submitter clinical testing

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