ClinVar Miner

Submissions for variant NC_000008.10:g.119379055_119379157TGAAA[149]TAAAA[446]

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Excellence Center for Genomics and Precision Medicine, King Chulalongkorn Memorial Hospital RCV001260916 SCV001237462 pathogenic Epilepsy, familial adult myoclonic, 1 2020-04-15 no assertion criteria provided research

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