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
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
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
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25