ClinVar Miner

Submissions for variant NM_001605.3(AARS1):c.783C>T (p.Asp261=)

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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 RCV005173236 SCV005797999 likely benign Charcot-Marie-Tooth disease type 2 2025-01-23 criteria provided, single submitter clinical testing

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