ClinVar Miner

Submissions for variant GRCh37/hg19 5q14.3(chr5:89940237-89999954)x1

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Lineagen, Inc RCV000848447 SCV000990589 pathogenic not provided 2018-08-08 no assertion criteria provided clinical testing
Lineagen, Inc RCV000848491 SCV000990633 pathogenic not provided 2018-08-08 no assertion criteria provided clinical testing
Lineagen, Inc RCV000850023 SCV000992165 uncertain significance not provided 2017-06-14 no assertion criteria provided clinical testing

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