ClinVar Miner

Submissions for variant GRCh38/hg38 15q11.2(chr15:22655582-23066575)x1

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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 1 RCV000050342 SCV000173127 conflicting data from submitters See cases 2014-07-18 no assertion criteria provided clinical testing Uncertain significance(13), Likely benign (1)
ISCA site 14 RCV000050342 SCV000173126 likely pathogenic See cases no assertion criteria provided clinical testing
ISCA site 2 RCV000050334 SCV000196167 benign See cases 2011-09-16 no assertion criteria provided clinical testing
ISCA site 4 RCV000148277 SCV000077641 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 4 RCV000148283 SCV000077649 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 4 RCV000050334 SCV000196168 benign See cases 2010-02-28 no assertion criteria provided clinical testing
ISCA site 6 RCV000051238 SCV000078583 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing

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