ClinVar Miner

Submissions for variant GRCh38/hg38 16p12.2(chr16:21826171-22396610)x1

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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 1 RCV000148150 SCV000190732 uncertain significance See cases 2011-05-06 no assertion criteria provided clinical testing
ISCA site 1 RCV000050398 SCV000196233 uncertain significance See cases 2014-12-19 no assertion criteria provided clinical testing
ISCA site 14 RCV000050398 SCV000175105 pathogenic/likely pathogenic See cases no assertion criteria provided clinical testing Pathogenic(1), Likely pathogenic(1)
ISCA site 14 RCV000148150 SCV000190733 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 17 RCV000050398 SCV000196234 uncertain significance See cases 2013-02-06 no assertion criteria provided clinical testing
ISCA site 4 RCV000148150 SCV000190734 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 4 RCV000050398 SCV000196235 uncertain significance See cases 2010-02-28 no assertion criteria provided clinical testing

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