ClinVar Miner

Submissions for variant GRCh38/hg38 22q11.22-11.23(chr22:22669543-24563859)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 4 RCV000148079 SCV000190805 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 4 RCV000050739 SCV000175297 pathogenic See cases 2010-05-27 no assertion criteria provided clinical testing
ISCA site 1 RCV000050739 SCV000175298 uncertain significance See cases 2011-02-18 no assertion criteria provided clinical testing

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