RS186476170 NDUFS2

Health Risk Chr 1:161213712
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
NDUFS2-related disorder
Inborn genetic diseases
NDUFS2-related disorder
Other Variants in NDUFS2
rs121434427 rs121434428 rs121434429 rs76309459 rs202121443 rs142594036 rs190184430 rs74124661 rs201554004 rs772424969
Ask Dr. Hemsworth about this variant