RS1193147148 NR2F1

Health Risk Chr 5:93585063
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in NR2F1
rs587777274 rs587777275 rs587777276 rs587777277 rs863224903 rs886039714 rs778199728 rs886041216 rs886041738 rs1057519434
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