Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs7124442 0.827 0.160 11 27655494 3 prime UTR variant C/G;T snv 9