ClinVar Miner

Submissions for variant GRCh38/hg38 15q13.3(chr15:31738809-32217725)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 4 RCV000148225 SCV000078045 benign See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 4 RCV000050713 SCV000175282 conflicting data from submitters See cases 2010-05-27 no assertion criteria provided clinical testing Uncertain significance(3), Benign (1)
ISCA site 17 RCV000050713 SCV000196295 uncertain significance See cases 2011-09-16 no assertion criteria provided clinical testing
ISCA site 8 RCV000050713 SCV000196296 uncertain significance See cases 2010-10-19 no assertion criteria provided clinical testing

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