RS2148373642 FHL1
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Associated Conditions
Myopathy
reducing body
X-linked
childhood-onset
early-onset
severe
X-linked myopathy with postural muscle atrophy
X-linked scapuloperoneal muscular dystrophy
Myopathy
reducing body
X-linked
childhood-onset
early-onset
severe
X-linked myopathy with postural muscle atrophy
Other Variants in FHL1