ClinVar Miner

Submissions for variant GRCh38/hg38 15q13.2-13.3(chr15:30361674-32222779)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 15 RCV000052433 SCV000079785 pathogenic See cases 2011-08-12 criteria provided, single submitter clinical testing

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