ClinVar Miner

Submissions for variant NM_000053.4(ATP7B):c.3412+1G>C

dbSNP: rs1957388064
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
National Institute of Allergy and Infectious Diseases - Centralized Sequencing Program, National Institutes of Health RCV002251695 SCV002522183 likely pathogenic Wilson disease 2021-08-06 criteria provided, single submitter clinical testing

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