ClinVar Miner

Submissions for variant NC_000011.10:g.(?_32389058)_(32435345_?)del

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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 RCV000653826 SCV000775716 pathogenic Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2021-09-09 criteria provided, single submitter clinical testing

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