ClinVar Miner

Submissions for variant NM_003060.4(SLC22A5):c.952-15_952-14insCGTATGA

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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 RCV003877322 SCV004684930 likely benign Renal carnitine transport defect 2023-09-25 criteria provided, single submitter clinical testing

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