RS797044957 DLAT

Health Risk Chr 11:112028603
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Pyruvate dehydrogenase E2 deficiency
Inborn genetic diseases
Pyruvate dehydrogenase E2 deficiency
Other Variants in DLAT
rs1862823765 rs781991355 rs143152014 rs782009811 rs1432866316 rs782807951 rs183829292 rs782185799 rs2498425963 rs782225633
Ask Dr. Hemsworth about this variant