RS786205225 NDUFB11

Health Risk Chr X:47142690
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What This Variant Does
"CLNSIG=5
Associated Conditions
Linear skin defects with multiple congenital anomalies 3
Histiocytoid cardiomyopathy
Linear skin defects with multiple congenital anomalies 1
Mitochondrial complex I deficiency
nuclear type 1
Linear skin defects with multiple congenital anomalies 3
Histiocytoid cardiomyopathy
Linear skin defects with multiple congenital anomalies 1
Mitochondrial complex I deficiency
nuclear type 1
Other Variants in NDUFB11
rs876657384 rs1057519073 rs150506634 rs1556760664 rs2147053098 rs202002020 rs199837826 rs2520209863 rs1556760660 rs2520209894
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