ClinVar Miner

Submissions for variant GRCh38/hg38 15q11.2(chr15:22572809-23066575)x1

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA Site 6 RCV000051236 SCV000078581 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 4 RCV000133674 SCV000173084 benign See cases 2010-05-27 no assertion criteria provided clinical testing
ISCA site 1 RCV000133674 SCV000173085 conflicting data from submitters See cases 2014-07-18 no assertion criteria provided clinical testing Uncertain significance(17), Likely benign (1)

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