ClinVar Miner

Submissions for variant GRCh38/hg38 15q13.2-13.3(chr15:30217122-32217725)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 2 RCV000141477 SCV000182394 pathogenic See cases 2013-02-04 no assertion criteria provided clinical testing

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