ClinVar Miner

Submissions for variant NM_178857.6(RP1L1):c.5610G>A (p.Glu1870=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003435443 SCV004159525 likely benign not provided 2024-12-01 criteria provided, single submitter clinical testing RP1L1: BP4, BP7

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