ClinVar Miner

Submissions for variant GRCh37/hg19 9q34.3(chr9:139390822-139403378)x1

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Laboratory of Genetics and Genomics,Cincinnati Children's Hospital Medical Center	RCV000753200	SCV000881536	benign	not provided	2013-04-22	no assertion criteria provided	clinical testing

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