RS122458145 FHL1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Myopathy
reducing body
X-linked
childhood-onset
X-linked myopathy with postural muscle atrophy
Myopathy
reducing body
X-linked
early-onset
severe
Myopathy
reducing body
X-linked
childhood-onset
X-linked myopathy with postural muscle atrophy
Other Variants in FHL1