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
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
rs2274567
CR1
0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 10
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs6721961 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
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
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs4711998 0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182