RS886041081 SLC25A4

Health Risk Chr 4:185144891
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type)
autosomal dominant
Mitochondrial disease
Inborn genetic diseases
Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type)
autosomal dominant
Mitochondrial disease
Inborn genetic diseases
Other Variants in SLC25A4
rs770816416 rs1163573848 rs2477166095 rs2477168490 rs142164891 rs1734410318 rs1734410152 rs1560841701 rs1553967481 rs886059266
Ask Dr. Hemsworth about this variant