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
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1805094 0.716 0.440 1 65610269 missense variant G/C;T snv 0.16; 4.0E-06 16
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1800247 0.882 0.200 1 156242034 intron variant T/C snv 0.20 4
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306