Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1980493 0.776 0.400 6 32395438 intron variant T/C snv 0.13 10
rs2516049 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 12
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs562962093 0.742 0.520 10 52771740 upstream gene variant T/C snv 7.0E-06 13
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs4684677 0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82