ClinVar Miner

Submissions for variant GRCh38/hg38 11q22.1(chr11:97849768-98439058)x1

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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 1 RCV000135751 SCV000175705 conflicting data from submitters See cases 2011-08-05 no assertion criteria provided clinical testing Uncertain significance(2), Likely benign (1)
ISCA site 2 RCV000135751 SCV000196345 benign See cases 2013-02-04 no assertion criteria provided clinical testing
ISCA site 8 RCV000135751 SCV000196346 benign See cases 2010-10-19 no assertion criteria provided clinical testing

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