ClinVar Miner

Submissions for variant GRCh38/hg38 1q21.3(chr1:153641117-153752390)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 15 RCV000148158 SCV000078878 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 8 RCV000051530 SCV000175399 benign See cases 2010-10-14 no assertion criteria provided clinical testing

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