ClinVar Miner

Submissions for variant NM_014845.6(FIG4):c.446+21dup

dbSNP: rs1321436747
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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 RCV002210266 SCV002366986 likely benign Charcot-Marie-Tooth disease type 4 2023-08-04 criteria provided, single submitter clinical testing

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