RS1557045066 SLC6A8

Health Risk Chr X:153693368
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Creatine transporter deficiency
Inborn genetic diseases
Creatine transporter deficiency
Other Variants in SLC6A8
rs122453113 rs122453114 rs80338740 rs1569539359 rs1569539244 rs122453116 rs122453117 rs122453118 rs80338739 rs397515558
Ask Dr. Hemsworth about this variant