Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1050501 0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs1059288 0.882 0.320 6 33299895 3 prime UTR variant A/G snv 0.60 3
rs1063320 0.752 0.360 6 29830972 3 prime UTR variant C/G;T snv 12
rs1063355 0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 5
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1738074 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58