ClinVar Miner

Submissions for variant NM_000053.4(ATP7B):c.1869+18_1869+20del

dbSNP: rs758773114
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001997051 SCV002227412 likely benign Wilson disease 2024-11-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001997051 SCV002782615 uncertain significance Wilson disease 2022-05-18 criteria provided, single submitter clinical testing

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