ClinVar Miner

Submissions for variant GRCh38/hg38 2q13(chr2:110104900-110201550)x1

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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 RCV000135460 SCV000175181 uncertain significance See cases 2009-07-30 no assertion criteria provided clinical testing
ISCA site 8 RCV000135460 SCV000175180 benign See cases 2010-10-20 no assertion criteria provided clinical testing

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