ClinVar Miner

Submissions for variant NM_006343.3(MERTK):c.2227G>A (p.Gly743Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV003990571 SCV004807343 likely pathogenic Retinitis pigmentosa 38 2024-03-26 criteria provided, single submitter clinical testing

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