RS115079861 RMND1

Health Risk Chr 6:151405236
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Combined oxidative phosphorylation defect type 11
Mitochondrial disease
Inborn genetic diseases
Combined oxidative phosphorylation defect type 11
Mitochondrial disease
Inborn genetic diseases
Other Variants in RMND1
rs1562800908 rs397515421 rs144972972 rs606231472 rs886037773 rs886037771 rs773470671 rs771894262 rs886037772 rs370863743
Ask Dr. Hemsworth about this variant