ClinVar Miner

Submissions for variant GRCh38/hg38 9p24.3(chr9:204193-295405)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 4 RCV000148192 SCV000077737 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 17 RCV000050426 SCV000175127 benign See cases 2009-07-30 no assertion criteria provided clinical testing

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