RS41284307 SELENON

Health Risk Chr 1:25814192
Upload your DNA to see your genotype for this variant.
Associated Conditions
SEPN1-related disorder
Eichsfeld type congenital muscular dystrophy
SEPN1-related disorder
Eichsfeld type congenital muscular dystrophy
Other Variants in SELENON
rs121908182 rs587776597 rs121908184 rs121908185 rs121908186 rs368104077 rs121908187 rs121908188 rs398124359 rs377215510
Ask Dr. Hemsworth about this variant