ClinVar Miner

Submissions for variant GRCh38/hg38 4q35.2(chr4:189111218-189975519)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 RCV000050473 SCV000175201 benign See cases 2009-07-30 no assertion criteria provided clinical testing
ISCA site 1 RCV000050473 SCV000175202 uncertain significance See cases 2010-12-22 no assertion criteria provided clinical testing

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