RS1555446980 NR2F2

Health Risk Chr 15:96332169
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in NR2F2
rs2505780251 rs2505770216 rs2505774176 rs201527820 rs2505774793 rs2505779992 rs2505775271 rs2505774216 rs2505774507 rs2505780323
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