ClinVar Miner

Submissions for variant GRCh38/hg38 15q13.2-13.3(chr15:30438310-32607357)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 RCV000135452 SCV000175166 pathogenic See cases 2009-07-30 no assertion criteria provided clinical testing
ISCA site 1 RCV000135452 SCV000175167 uncertain significance See cases 2010-12-22 no assertion criteria provided clinical testing

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