ClinVar Miner

Submissions for variant GRCh38/hg38 7q21.13(chr7:89030468-89447599)x1

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 1 RCV000509061 SCV000080041 uncertain significance See cases 2011-05-06 no assertion criteria provided clinical testing
ISCA site 1 RCV000052687 SCV000181432 conflicting data from submitters See cases 2013-04-04 no assertion criteria provided clinical testing Uncertain significance(2), Likely benign (1)

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