ClinVar Miner

Submissions for variant NM_018238.4(AGK):c.411A>T (p.Arg137=)

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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 RCV003794120 SCV004583036 likely benign Sengers syndrome; Cataract 38 2023-06-15 criteria provided, single submitter clinical testing

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