ClinVar Miner

Submissions for variant NM_001025603.2(RFX5):c.939G>A (p.Ser313=)

dbSNP: rs1319132683
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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 RCV001430830 SCV001633575 likely benign MHC class II deficiency 2020-08-02 criteria provided, single submitter clinical testing

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