RS773496318 NDUFA13

Health Risk Chr 19:19527294
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Associated Conditions
Mitochondrial complex I deficiency
nuclear type 28
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 28
Inborn genetic diseases
Other Variants in NDUFA13
rs137852869 rs752513525 rs183288709 rs2061105702 rs2061098856 rs751852332 rs779602473
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