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member pro789 Cytochrome P450 Family 24 Subfamily A Member 1, Protein Coding, DISEASES Pro789=) SNV, Benign · 468597 · rs372737275 GRCh37: 19:42,474,591-42,474,591 

member pro789 Developmental and epileptic encephalopathy, 1; Autosomal dominant nonsyndromic hearing loss 65; Caused by mutation in the TBC1 domain family, member 24 

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