ClinVar Miner

Submissions for variant GRCh37/hg19 17q12(chr17:34822465-36410559)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 RCV000511856 SCV000584585 likely pathogenic See cases 2014-12-02 no assertion criteria provided clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV001259334 SCV001436303 pathogenic not provided 2020-04-29 no assertion criteria provided clinical testing

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