RS747166010 TTC19

Health Risk Chr 17:16006548
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial complex III deficiency nuclear type 2
Inborn genetic diseases
Mitochondrial complex III deficiency nuclear type 2
Inborn genetic diseases
Other Variants in TTC19
rs387907094 rs794726691 rs794726692 rs77955179 rs2302414 rs774176392 rs769078093 rs756830714 rs779592523 rs544027755
Ask Dr. Hemsworth about this variant