ClinVar Miner

Submissions for variant GRCh37/hg19 17p13.3(chr17:525-632905)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 RCV000510587 SCV000584554 conflicting data from submitters See cases 2015-06-22 no assertion criteria provided clinical testing Uncertain significance(1), Likely benign (1)
Lineagen, Inc RCV000847156 SCV000989278 uncertain significance not provided 2017-12-27 no assertion criteria provided clinical testing
Lineagen, Inc RCV000848422 SCV000990564 uncertain significance not provided 2017-09-07 no assertion criteria provided clinical testing

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