ClinVar Miner

Submissions for variant NM_001625.4(AK2):c.219+20T>C

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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 RCV003850090 SCV004653563 likely benign Reticular dysgenesis 2023-03-23 criteria provided, single submitter clinical testing

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