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
rs3820589 0.925 0.200 1 42960373 intron variant A/T snv 8.3E-02 2
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
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
rs17300539 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs3773885
MME
0.925 0.200 3 155141792 intron variant G/A snv 0.33 2
rs3796268
MME
0.925 0.200 3 155117435 intron variant T/C snv 0.30 2
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs58624704
ALB
0.925 0.200 4 73410325 missense variant G/A snv 8.0E-06 3.5E-05 2
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1567438 0.925 0.200 6 160458599 intron variant T/C snv 0.25 3
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs2457576 0.925 0.200 6 160444587 intron variant G/C snv 0.27 2
rs316019 0.790 0.360 6 160249250 missense variant A/C snv 0.90 0.89 8
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246