RS34526199 AMPD1

Health Risk Chr 1:114679616
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What This Variant Does
"CLNSIG=5
Associated Conditions
Muscle AMP deaminase deficiency
Hypercholesterolemia
autosomal dominant
type B
AMPD1-related disorder
Muscle AMP deaminase deficiency
Hypercholesterolemia
autosomal dominant
type B
AMPD1-related disorder
Other Variants in AMPD1
rs17602729 rs35859650 rs121912682 rs61752479 rs61752478 rs398123114 rs398123115 rs146422068 rs61741025 rs139582106
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