ClinVar Miner

Submissions for variant NC_000023.9:g.146703942_146820448del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Elsea Lab, Dept of Molecular and Human Genetics,Baylor College of Medicine RCV000162202 SCV000172267 pathogenic Fragile X syndrome 2014-06-05 no assertion criteria provided research

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