RS763765943 SLC6A19

Health Risk Chr 5:1219528
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Neutral 1 amino acid transport defect
Inborn genetic diseases
Neutral 1 amino acid transport defect
Other Variants in SLC6A19
rs778611489 rs121434346 rs121434347 rs369804798 rs142979576 rs1554033750 rs1561165786 rs762942358 rs756010661 rs149124864
Ask Dr. Hemsworth about this variant