ClinVar Miner

List of variants in gene FHL1 studied for Myopathy, reducing body, X-linked, childhood-onset; Myopathy, reducing body, X-linked, early-onset, severe; Myopathy with postural muscle atrophy, X-linked; Uruguay faciocardiomusculoskeletal syndrome; Scapuloperoneal myopathy, X-linked dominant

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Total variants: 1
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NM_001159699.2(FHL1):c.496T>C (p.Cys166Arg) rs1603271659

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