ClinVar Miner

Submissions for variant NM_001365999.1(SZT2):c.2929+15C>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biochemical Molecular Genetic Laboratory,King Abdulaziz Medical City RCV000723351 SCV000854750 uncertain significance Early infantile epileptic encephalopathy 18 2018-08-23 no assertion criteria provided clinical testing

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