ClinVar Miner

Submissions for variant GRCh38/hg38 2p22.3(chr2:32452646-33032447)x3

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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 RCV000050870 SCV000175326 conflicting data from submitters See cases 2011-08-05 no assertion criteria provided clinical testing Uncertain significance(6), Likely benign (3)
ISCA site 4 RCV000050870 SCV000175325 benign See cases 2013-06-25 no assertion criteria provided clinical testing
ISCA site 4 RCV000148094 SCV000190825 benign See cases 2011-08-12 criteria provided, single submitter clinical testing

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