Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83