RS749196122 TTC19

Health Risk Chr 17:15999849
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Associated Conditions
Inborn genetic diseases
Mitochondrial complex III deficiency nuclear type 2
Inborn genetic diseases
Mitochondrial complex III deficiency nuclear type 2
Other Variants in TTC19
rs747166010 rs387907094 rs794726691 rs794726692 rs77955179 rs2302414 rs774176392 rs769078093 rs756830714 rs779592523
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