RS119480071 LPIN1

Health Risk Chr 2:11773666
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Myoglobinuria
acute recurrent
autosomal recessive
Myoglobinuria
acute recurrent
autosomal recessive
Other Variants in LPIN1
rs119480072 rs119480073 rs730880306 rs398124543 rs886041544 rs145629147 rs777607912 rs146529487 rs200898383 rs114931326
Ask Dr. Hemsworth about this variant