ClinVar Miner

Submissions for variant NM_001349338.3(FOXP1):c.*1231_*1235dup

dbSNP: rs373349025
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000407204 SCV000446088 uncertain significance Intellectual Disability with Language Impairment and Autistic Features 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003430887 SCV004150472 benign not provided 2022-10-01 criteria provided, single submitter clinical testing FOXP1: BS1, BS2

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