ClinVar Miner

Submissions for variant GRCh38/hg38 7q21.13(chr7:88563550-90170632)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 RCV000148087 SCV000190796 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 1 RCV000050715 SCV000175285 conflicting data from submitters See cases 2011-10-10 no assertion criteria provided clinical testing Uncertain significance(2), Likely benign (1)
ISCA site 4 RCV000050715 SCV000175286 uncertain significance See cases 2010-02-28 no assertion criteria provided clinical testing

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