ClinVar Miner

Submissions for variant NM_014491.4(FOXP2):c.*229dup

dbSNP: rs543811999
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000297509 SCV000466361 benign Childhood apraxia of speech 2016-06-14 criteria provided, single submitter clinical testing

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