ClinVar Miner

Submissions for variant NM_014009.4(FOXP3):c.331G>A (p.Ala111Thr)

gnomAD frequency: 0.00004  dbSNP: rs1424687079
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002023375 SCV002307047 likely benign Insulin-dependent diabetes mellitus secretory diarrhea syndrome 2022-07-11 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002023375 SCV002816437 uncertain significance Insulin-dependent diabetes mellitus secretory diarrhea syndrome 2022-04-05 criteria provided, single submitter clinical testing

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