ClinVar Miner

Submissions for variant GRCh38/hg38 15q11.2(chr15:22572809-23066575)x3

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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 17 RCV000135477 SCV000196262 benign See cases 2009-07-30 no assertion criteria provided clinical testing
ISCA site 4 RCV000135477 SCV000196263 benign See cases 2010-01-30 no assertion criteria provided clinical testing
ISCA site 8 RCV000135477 SCV000175214 uncertain significance See cases 2010-10-19 no assertion criteria provided clinical testing

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