ClinVar Miner

Submissions for variant GRCh38/hg38 15q13.2-13.3(chr15:30662523-32217725)x1

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 17 RCV000148066 SCV000190741 pathogenic See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 4 RCV000148066 SCV000190742 pathogenic See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 1 RCV000050442 SCV000196242 pathogenic See cases 2010-12-22 no assertion criteria provided clinical testing
ISCA site 17 RCV000050442 SCV000196243 pathogenic See cases 2009-07-30 no assertion criteria provided clinical testing
ISCA site 2 RCV000050442 SCV000196244 pathogenic See cases 2013-02-04 no assertion criteria provided clinical testing

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