RS1050852336 SELENON

Health Risk Chr 1:25800289
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Associated Conditions
Eichsfeld type congenital muscular dystrophy
Inborn genetic diseases
Eichsfeld type congenital muscular dystrophy
Inborn genetic diseases
Other Variants in SELENON
rs121908182 rs587776597 rs121908184 rs121908185 rs121908186 rs368104077 rs121908187 rs121908188 rs398124359 rs377215510
Ask Dr. Hemsworth about this variant