ClinVar Miner

Submissions for variant NM_014009.4(FOXP3):c.455-6C>T

gnomAD frequency: 0.00018  dbSNP: rs373767482
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000734388 SCV000862524 uncertain significance not provided 2018-07-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067167 SCV002386515 benign Insulin-dependent diabetes mellitus secretory diarrhea syndrome 2023-12-21 criteria provided, single submitter clinical testing

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