ClinVar Miner

Submissions for variant NM_014009.4(FOXP3):c.736-1G>A

dbSNP: rs1602684221
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne RCV000825005 SCV000966197 likely pathogenic Insulin-dependent diabetes mellitus secretory diarrhea syndrome 2018-08-21 criteria provided, single submitter clinical testing

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