ClinVar Miner

Submissions for variant NM_000096.4(CP):c.2554+15G>A

dbSNP: rs751719558
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002017072 SCV002300287 likely benign Deficiency of ferroxidase 2024-03-04 criteria provided, single submitter clinical testing

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