ClinVar Miner

Submissions for variant NM_014009.4(FOXP3):c.340C>T (p.Arg114Trp)

gnomAD frequency: 0.00023  dbSNP: rs200554980
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000501041 SCV000594878 uncertain significance not specified 2016-02-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000970540 SCV001118125 benign Insulin-dependent diabetes mellitus secretory diarrhea syndrome 2024-01-28 criteria provided, single submitter clinical testing

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