ClinVar Miner

Submissions for variant NM_014845.6(FIG4):c.2097-10C>T (rs142482745)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000862182 SCV001002648 likely benign not provided 2018-12-20 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001173273 SCV001336356 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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