RS567452162 ARHGEF18

Health Risk Chr 19:7470002
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in ARHGEF18
rs987233144 rs1064793000 rs1064793001 rs767689418 rs1064793002 rs199567237 rs531485198 rs115555106 rs116148705 rs180746700
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