ClinVar Miner

Submissions for variant GRCh38/hg38 16p13.11(chr16:14816348-16580464)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 1 RCV000135525 SCV000175395 uncertain significance See cases 2012-03-09 no assertion criteria provided clinical testing
ISCA site 1 RCV000148114 SCV000175396 pathogenic See cases 2011-05-06 no assertion criteria provided clinical testing

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