ClinVar Miner

Submissions for variant NM_000843.4(GRM6):c.2236_2237del (p.Met746fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV003990840 SCV004807844 likely pathogenic Congenital stationary night blindness 1B 2024-03-29 criteria provided, single submitter clinical testing

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