ClinVar Miner

Submissions for variant NM_000053.4(ATP7B):c.447G>A (p.Val149=)

dbSNP: rs776619662
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 RCV001428543 SCV001631243 likely benign Wilson disease 2024-01-22 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001428543 SCV005635250 uncertain significance Wilson disease 2024-02-19 criteria provided, single submitter clinical testing

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