RS80338740 SLC6A8

Health Risk Chr X:153693979
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What This Variant Does
"X-linked creatine deficiency syndrome: a novel mutation in creatine transporter gene SLC6A8. [OMIM:...
Associated Conditions
Creatine transporter deficiency
Creatine transporter deficiency
Other Variants in SLC6A8
rs122453113 rs122453114 rs1569539359 rs1569539244 rs122453116 rs122453117 rs122453118 rs80338739 rs397515558 rs397515559
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