ClinVar Miner

Submissions for variant GRCh37/hg19 16p12.2(chr16:21801889-22431357)x3

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 1 RCV000511874 SCV000586678 conflicting data from submitters See cases 2016-02-29 no assertion criteria provided clinical testing Uncertain significance(2), Likely benign (1)
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000683789 SCV000811298 uncertain significance not provided 2021-01-20 no assertion criteria provided clinical testing

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