ClinVar Miner

List of variants reported as likely pathogenic for Sensorineural hearing loss; Rod-cone dystrophy; Adult Fanconi syndrome by Ramesar Group, Division of Human Genetics, Institute of Infectious Diseases and Molecular Medicine,UCT/MRC Genomic and Precision Medicine Research Unit, University of Cape Town

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Total variants: 1
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NM_015713.5(RRM2B):c.786G>T (p.Glu262Asp)

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