ClinVar Miner

Submissions for variant NM_000096.4(CP):c.782-9G>T

dbSNP: rs566719310
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002083306 SCV002376132 likely benign Deficiency of ferroxidase 2022-07-05 criteria provided, single submitter clinical testing

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