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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2279590
CLU
0.851 0.200 8 27598736 non coding transcript exon variant T/C snv 0.69 5
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
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
rs4746 0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs4151667 0.790 0.320 6 31946247 missense variant T/A snv 3.9E-02 3.4E-02 9
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
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
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs7493 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
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
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249