ClinVar Miner

Submissions for variant GRCh37/hg19 16p13.3(chr16:6294808-6394422)x1

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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 RCV000512245 SCV000585047 likely benign See cases 2014-07-18 no assertion criteria provided clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000683754 SCV000811263 uncertain significance not provided 2017-06-09 no assertion criteria provided clinical testing
Lineagen Inc. RCV000849629 SCV000991771 uncertain significance not provided 2018-07-20 no assertion criteria provided clinical testing

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