RS146048019 LPIN1

Health Risk Chr 2:11802992
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Associated Conditions
Myoglobinuria
acute recurrent
autosomal recessive
Inborn genetic diseases
Myoglobinuria
acute recurrent
autosomal recessive
Inborn genetic diseases
Other Variants in LPIN1
rs119480071 rs119480072 rs119480073 rs730880306 rs398124543 rs886041544 rs145629147 rs777607912 rs146529487 rs200898383
Ask Dr. Hemsworth about this variant