RS80338739 SLC6A8

Health Risk Chr X:153690428
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What This Variant Does
"CLNSIG=5
Associated Conditions
Creatine transporter deficiency
Inborn genetic diseases
Creatine transporter deficiency
Inborn genetic diseases
Other Variants in SLC6A8
rs122453113 rs122453114 rs80338740 rs1569539359 rs1569539244 rs122453116 rs122453117 rs122453118 rs397515558 rs397515559
Ask Dr. Hemsworth about this variant