ClinVar Miner

Submissions for variant GRCh38/hg38 15q13.2-13.3(chr15:30438310-32569425)x3

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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 17 RCV000148179 SCV000077684 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 1 RCV000050375 SCV000174558 conflicting data from submitters See cases 2011-10-07 no assertion criteria provided clinical testing Pathogenic(1), Uncertain significance(2)

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