RS587777255 SLC38A8

Health Risk Chr 16:84016679
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What This Variant Does
"CLNSIG=5
Associated Conditions
FOVEAL HYPOPLASIA 2 WITH OPTIC NERVE MISROUTING AND ANTERIOR SEGMENT DYSGENESIS
Inborn genetic diseases
FOVEAL HYPOPLASIA 2 WITH OPTIC NERVE MISROUTING AND ANTERIOR SEGMENT DYSGENESIS
Inborn genetic diseases
Other Variants in SLC38A8
rs587777253 rs587777254 rs587777256 rs372929441 rs149592537 rs587777257 rs1057516193 rs139373929 rs1057521634 rs760391436
Ask Dr. Hemsworth about this variant