ClinVar Miner

Submissions for variant NM_000053.4(ATP7B):c.2865+1G>A (rs587783306)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory,University of Chicago RCV000145266 SCV000192333 pathogenic Wilson disease 2013-02-08 criteria provided, single submitter clinical testing
Counsyl RCV000145266 SCV000485317 likely pathogenic Wilson disease 2015-11-19 criteria provided, single submitter clinical testing

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