ClinVar Miner

Submissions for variant NM_014845.6(FIG4):c.1039+8G>A

dbSNP: rs2128386984
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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 RCV001467017 SCV001671028 likely benign Charcot-Marie-Tooth disease type 4 2020-09-20 criteria provided, single submitter clinical testing

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