RS561005562 SLC39A4

Health Risk Chr 8:144415026
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Associated Conditions
Inborn genetic diseases
Hereditary acrodermatitis enteropathica
Inborn genetic diseases
Hereditary acrodermatitis enteropathica
Other Variants in SLC39A4
rs2130796648 rs2130798769 rs781908504 rs121434287 rs121434288 rs121434289 rs121434290 rs121434291 rs2130797713 rs121434292
Ask Dr. Hemsworth about this variant