RS886041544 LPIN1

Health Risk Chr 2:11784887
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What This Variant Does
"CLNSIG=5
Associated Conditions
Myoglobinuria
acute recurrent
autosomal recessive
Myoglobinuria
acute recurrent
autosomal recessive
Other Variants in LPIN1
rs119480071 rs119480072 rs119480073 rs730880306 rs398124543 rs145629147 rs777607912 rs146529487 rs200898383 rs114931326
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