Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs1800044 0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03 8