RS782560726 SLC6A8

Health Risk Chr X:153695084
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Associated Conditions
Creatine transporter deficiency
Inborn genetic diseases
SLC6A8-related disorder
Creatine transporter deficiency
Inborn genetic diseases
SLC6A8-related disorder
Other Variants in SLC6A8
rs122453113 rs122453114 rs80338740 rs1569539359 rs1569539244 rs122453116 rs122453117 rs122453118 rs80338739 rs397515558
Ask Dr. Hemsworth about this variant