ClinVar Miner

Submissions for variant NM_003721.4(RFXANK):c.439-7C>T

gnomAD frequency: 0.00002  dbSNP: rs768383806
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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 RCV002080890 SCV002374332 likely benign MHC class II deficiency 2025-02-02 criteria provided, single submitter clinical testing

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