RS1603271659 FHL1

Health Risk Chr X:136207908
Upload your DNA to see your genotype for this variant.
Associated Conditions
Myopathy
reducing body
X-linked
childhood-onset
early-onset
severe
X-linked myopathy with postural muscle atrophy
Uruguay Faciocardiomusculoskeletal syndrome
X-linked scapuloperoneal muscular dystrophy
Myopathy
reducing body
X-linked
childhood-onset
early-onset
severe
Other Variants in FHL1
rs122458140 rs122458141 rs1603271580 rs122458142 rs122458143 rs122458144 rs122458145 rs122459146 rs122459147 rs122459148
Ask Dr. Hemsworth about this variant