RS121908184 SELENON

Health Risk Chr 1:25800231
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Eichsfeld type congenital muscular dystrophy
Congenital myopathy with fiber type disproportion
Eichsfeld type congenital muscular dystrophy
Congenital myopathy with fiber type disproportion
Other Variants in SELENON
rs121908182 rs587776597 rs121908185 rs121908186 rs368104077 rs121908187 rs121908188 rs398124359 rs377215510 rs149623434
Ask Dr. Hemsworth about this variant