ClinVar Miner

Submissions for variant NM_001625.4(AK2):c.219+16C>T

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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 RCV003875945 SCV004677587 likely benign Reticular dysgenesis 2022-11-07 criteria provided, single submitter clinical testing

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