RS1064794694 HSD17B10

Health Risk Chr X:53432035
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
HSD10 mitochondrial disease
Neurodevelopmental delay
Inborn genetic diseases
HSD10 mitochondrial disease
Neurodevelopmental delay
Other Variants in HSD17B10
rs374438347 rs782143488 rs2521096456 rs2521092158 rs2521092831 rs1348504554 rs2075834227 rs2075824424 rs1602426573 rs1556894502
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