RS760560618 RMND1

Health Risk Chr 6:151421322
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Associated Conditions
Inborn genetic diseases
Combined oxidative phosphorylation defect type 11
Inborn genetic diseases
Combined oxidative phosphorylation defect type 11
Other Variants in RMND1
rs1562800908 rs397515421 rs115079861 rs144972972 rs606231472 rs886037773 rs886037771 rs773470671 rs771894262 rs886037772
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