RS760101382 GAMT

Health Risk Chr 19:1398995
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cerebral creatine deficiency syndrome
Deficiency of guanidinoacetate methyltransferase
Inborn genetic diseases
Cerebral creatine deficiency syndrome
Deficiency of guanidinoacetate methyltransferase
Inborn genetic diseases
Other Variants in GAMT
rs80338736 rs80338734 rs121909272 rs104894694 rs80338735 rs796052525 rs370421531 rs753198836 rs796052527 rs747656257
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