ClinVar Miner

Submissions for variant GRCh38/hg38 1p36.33-36.32(chr1:844347-2627474)x1

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 14 RCV000148161 SCV000190806 pathogenic See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 4 RCV000148161 SCV000190807 pathogenic See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 2 RCV000050752 SCV000196301 pathogenic See cases 2011-09-16 no assertion criteria provided clinical testing
ISCA site 8 RCV000050752 SCV000196302 pathogenic See cases 2010-10-19 no assertion criteria provided clinical testing

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