ClinVar Miner

Submissions for variant NM_014009.4(FOXP3):c.552G>T (p.Ser184=)

dbSNP: rs782085584
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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 RCV001476923 SCV001681142 likely benign Insulin-dependent diabetes mellitus secretory diarrhea syndrome 2018-05-10 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001476923 SCV005682650 uncertain significance Insulin-dependent diabetes mellitus secretory diarrhea syndrome 2024-02-12 criteria provided, single submitter clinical testing

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