ClinVar Miner

Submissions for variant NM_014491.4(FOXP2):c.586C>T (p.Gln196Ter)

dbSNP: rs1347299046
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Lab, University of California San Francisco RCV001376007 SCV001573012 pathogenic Childhood apraxia of speech 2020-01-30 criteria provided, single submitter clinical testing

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