ClinVar Miner

Submissions for variant NM_014009.4(FOXP3):c.1221C>T (p.Thr407=)

gnomAD frequency: 0.00007  dbSNP: rs373302430
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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 RCV002186920 SCV002342126 benign Insulin-dependent diabetes mellitus secretory diarrhea syndrome 2024-01-04 criteria provided, single submitter clinical testing

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