RS587784384 SLC16A2

Health Risk Chr X:74525834
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What This Variant Does
"CLNSIG=5
Associated Conditions
Allan-Herndon-Dudley syndrome
Inborn genetic diseases
Spastic paraplegia
Hereditary spastic paraplegia
Allan-Herndon-Dudley syndrome
Inborn genetic diseases
Spastic paraplegia
Hereditary spastic paraplegia
Other Variants in SLC16A2
rs104894931 rs2519806849 rs104894936 rs122455132 rs104894938 rs104894939 rs104894940 rs387906501 rs113994166 rs367543059
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