ClinVar Miner

Submissions for variant NM_005762.3(TRIM28):c.39C>T (p.Ala13=)

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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 RCV005110553 SCV005728182 likely benign not provided 2024-03-21 criteria provided, single submitter clinical testing

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