ClinVar Miner

Submissions for variant NM_000096.4(CP):c.1714-13_1714-9del

dbSNP: rs2108244342
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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 RCV002196627 SCV002492225 likely benign Deficiency of ferroxidase 2021-11-09 criteria provided, single submitter clinical testing

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