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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
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
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1569355102 0.695 0.360 21 37472869 frameshift variant TAAC/- delins 51
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1555462347 0.716 0.520 16 8901028 frameshift variant CT/- delins 34
rs370717845 0.763 0.320 8 43161462 missense variant G/A snv 33