ClinVar Miner

Submissions for variant NM_014009.4(FOXP3):c.116G>A (p.Arg39Gln)

gnomAD frequency: 0.00002  dbSNP: rs782639786
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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 RCV001515914 SCV001724096 benign Insulin-dependent diabetes mellitus secretory diarrhea syndrome 2020-02-17 criteria provided, single submitter clinical testing

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