Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs17036188 0.882 0.120 3 12299426 intron variant T/C snv 4.0E-02 3
rs497116 0.925 0.080 11 104892390 stop lost A/G snv 4.3E-02 2
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs77874543 0.882 0.080 22 41926712 missense variant G/C;T snv 6.1E-02 5.5E-02 3
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs885479 0.732 0.280 16 89919746 missense variant G/A snv 0.15 8.3E-02 16
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs10506481 0.882 0.080 12 66250331 3 prime UTR variant T/C snv 9.0E-02 3
rs12605436 0.925 0.080 18 35906684 upstream gene variant C/T snv 9.1E-02 2
rs867186 0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 15
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs12048215 0.882 0.160 1 247421289 intron variant A/G snv 0.11 3
rs8177374 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs1800450 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs2808530 0.925 0.080 9 98576823 intron variant A/C snv 0.12 2
rs2234237 0.763 0.280 6 41282728 missense variant T/A snv 0.13 0.12 9
rs2232618
LBP
0.851 0.160 20 38373117 missense variant T/C snv 9.2E-02 0.12 5
rs8177375 0.925 0.080 11 126293169 3 prime UTR variant A/G snv 0.12 0.13 2