ClinVar Miner

Submissions for variant GRCh38/hg38 22q11.23(chr22:23377984-24563859)x3

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 1 RCV000053179 SCV000175679 uncertain significance See cases 2011-09-12 no assertion criteria provided clinical testing
ISCA site 14 RCV000148169 SCV000190904 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 17 RCV000148169 SCV000190905 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 4 RCV000053179 SCV000175678 pathogenic See cases 2010-03-30 no assertion criteria provided clinical testing

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