RS587777257 SLC38A8

Health Risk Chr 16:84017246
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Foveal hypoplasia 2 and optic nerve misrouting with or without anterior segment dysgenesis
Foveal hypoplasia 2 and optic nerve misrouting with or without anterior segment dysgenesis
Other Variants in SLC38A8
rs587777253 rs587777254 rs587777255 rs587777256 rs372929441 rs149592537 rs1057516193 rs139373929 rs1057521634 rs760391436
Ask Dr. Hemsworth about this variant