ClinVar Miner

Submissions for variant NM_205861.3(DHDDS):c.766-20T>C

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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 RCV003641981 SCV004521713 likely benign Retinitis pigmentosa 59 2023-08-30 criteria provided, single submitter clinical testing

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