ClinVar Miner

Submissions for variant NM_014009.4(FOXP3):c.873C>T (p.Val291=)

gnomAD frequency: 0.00005  dbSNP: rs782371089
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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 RCV002125791 SCV002450308 benign Insulin-dependent diabetes mellitus secretory diarrhea syndrome 2024-01-08 criteria provided, single submitter clinical testing

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