ClinVar Miner

Submissions for variant GRCh38/hg38 6q25.3(chr6:156965417-157093452)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 1 RCV000138665 SCV000179050 pathogenic See cases 2012-06-11 no assertion criteria provided clinical testing

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