RS144972972 RMND1

Health Risk Chr 6:151430154
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial disease
Combined oxidative phosphorylation defect type 11
Mitochondrial oxidative phosphorylation disorder
Nephronophthisis
Inborn genetic diseases
Mitochondrial disease
Combined oxidative phosphorylation defect type 11
Mitochondrial oxidative phosphorylation disorder
Nephronophthisis
Inborn genetic diseases
Other Variants in RMND1
rs1562800908 rs397515421 rs115079861 rs606231472 rs886037773 rs886037771 rs773470671 rs771894262 rs886037772 rs370863743
Ask Dr. Hemsworth about this variant