ClinVar Miner

Submissions for variant GRCh38/hg38 3p24.1(chr3:30638613-30656356)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 14 RCV000053928 SCV000081291 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing

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