ClinVar Miner

Submissions for variant NM_003721.4(RFXANK):c.702A>T (p.Gly234=)

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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 RCV003636403 SCV004513952 likely benign MHC class II deficiency 2023-05-23 criteria provided, single submitter clinical testing

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