RS139373929 SLC38A8

Health Risk Chr 16:84017245
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
Inborn genetic diseases
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
Inborn genetic diseases
Other Variants in SLC38A8
rs587777253 rs587777254 rs587777255 rs587777256 rs372929441 rs149592537 rs587777257 rs1057516193 rs1057521634 rs760391436
Ask Dr. Hemsworth about this variant