ClinVar Miner

Submissions for variant 9q21.13 deletion

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neurogenetics group, VIB, Antwerp, Belgium RCV000208776 SCV000264654 likely pathogenic Epilepsy, childhood absence, susceptibility to, 1; Idiopathic generalized epilepsy 2016-02-10 no assertion criteria provided literature only

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