ClinVar Miner

Submissions for variant GRCh38/hg38 8p23.1(chr8:7411297-8222398)x3

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 4 RCV000148230 SCV000077805 benign See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 4 RCV000050484 SCV000175205 benign See cases 2013-09-18 no assertion criteria provided clinical testing
ISCA site 8 RCV000050484 SCV000175206 uncertain significance See cases 2010-10-19 no assertion criteria provided clinical testing

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