RS28939714 NDUFS3

Health Risk Chr 11:47582140
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY]
Associated Conditions
Mitochondrial complex I deficiency
nuclear type 8
Neurodevelopmental delay
Mitochondrial complex I deficiency
nuclear type 8
Neurodevelopmental delay
Other Variants in NDUFS3
rs377323760 rs778409332 rs2509732182 rs2509726707 rs2509726477 rs2153795389 rs3740654 rs138867882 rs770306617 rs104894270
Ask Dr. Hemsworth about this variant