ClinVar Miner

Submissions for variant NM_000538.4(RFXAP):c.606T>C (p.Ser202=)

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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 RCV002717007 SCV003011071 likely benign MHC class II deficiency 2022-02-20 criteria provided, single submitter clinical testing

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