RS2519929717 AP1S2

Health Risk Chr X:15852457
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in AP1S2
rs2519915767 rs1934288587 rs1933972061 rs1934209113 rs2519929746 rs1934205000 rs2519914292 rs2519914351 rs2519929432 rs1555904878
Ask Dr. Hemsworth about this variant