Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4149313 0.763 0.240 9 104824472 missense variant T/C snv 9
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1314386070 0.827 0.240 8 90042766 missense variant T/C snv 1.4E-05 9
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs2066715 0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02 7
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28