RS1085307599 EDA

Health Risk Chr X:70035364
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in EDA
rs132630308 rs132630309 rs132630310 rs132630311 rs132630312 rs132630313 rs132630314 rs132630315 rs132630316 rs132630317
Ask Dr. Hemsworth about this variant