ClinVar Miner

Submissions for variant NM_000843.4(GRM6):c.1501-1G>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ophthalmic Genetics Group, Institute of Molecular and Clinical Ophthalmology Basel RCV004795299 SCV005415491 pathogenic Retinal dystrophy 2024-05-27 criteria provided, single submitter research

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