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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62