ClinVar Miner

Submissions for variant NM_001025603.2(RFX5):c.1266C>T (p.Asp422=)

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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 RCV003637075 SCV004409023 likely benign MHC class II deficiency 2022-11-06 criteria provided, single submitter clinical testing

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