| Max Magnitude | Chromosome position | Summary |
---|
i5012770 | | | |
rs1057516320 | 0 | 89,981,430 | |
rs1057516321 | 0 | 89,982,721 | |
rs1057516332 | 0 | 89,953,501 | |
rs1057516392 | 0 | 89,981,516 | |
rs1057516611 | 0 | 89,947,890 | |
rs1057516668 | 0 | 89,946,236 | |
rs1057516772 | 0 | 89,982,719 | |
rs1057516787 | 0 | 89,978,273 | |
rs1057516852 | 0 | 89,946,209 | |
rs1057516869 | 0 | 89,946,160 | |
rs1057517075 | 0 | 89,946,138 | |
rs1057517102 | 0 | 89,955,556 | |
rs1057517104 | 0 | 89,971,172 | |
rs1057517209 | 0 | 89,958,724 | |
rs1057517262 | 0 | 89,937,076 | |
rs1057519585 | 0 | 89,980,884 | |
rs1057519586 | 0 | 89,971,194 | |
rs1057519587 | 0 | 89,964,480 | |
rs1057519588 | 0 | 89,955,555 | |
rs1060503463 | 0 | 89,980,831 | |
rs1060503466 | 0 | 89,947,881 | |
rs1060503467 | 0 | 89,955,282 | |
rs1060503480 | 0 | 89,953,536 | |
rs1060503481 | 0 | 89,953,438 | |
rs1060503485 | 0 | 89,984,536 | |
rs1061302 | 0 | 89,946,194 | |
rs1063054 | 0 | 89,934,373 | |
rs1064793210 | 0 | 89,984,551 | |
rs1064795634 | 0 | 89,981,480 | |
rs1064795816 | 0 | 89,943,276 | |
rs121908973 | 0 | 89,964,428 | |
rs121908974 | 0 | 89,958,760 | |
rs13312840 | 0 | 89,985,681 | |
rs142301194 | 0 | 89,937,024 | |
rs1805794 | 0 | 89,978,251 | |
rs1805812 | 0 | 89,952,825 | |
rs200287925 | 0 | 89,982,766 | |
rs2735383 | 0 | 89,935,041 | |
rs2735385 | 0 | 89,937,496 | |
rs34767364 | 0 | 89,971,232 | |
rs574673404 | 0 | 89,984,524 | |
rs587776650 | 6 | 89,971,214 | |
rs587780096 | 0 | 89,980,889 | |
rs587780100 | 0 | 89,971,174 | |
rs587781305 | 0 | 89,981,389 | |
rs587781718 | 0 | 89,982,804 | |
rs587781891 | 0 | 89,982,770 | |
rs587781969 | 0 | 89,955,538 | |
rs587782130 | 0 | 89,953,615 | |
NBN codes for nibrin, a protein with several vital roles within cells, such as DNA repair.
A variant, 657del5 at i5012770, is associated with Nijmegen breakage syndrome. 23andMe reports on this condition.