Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs4833095 0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs10719 0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs1532268 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 12
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2735940 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 25
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2736109 0.851 0.120 5 1296644 upstream gene variant C/T snv 0.32 4
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
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
rs752681512 0.851 0.120 5 7897088 missense variant A/G snv 2.0E-05 4
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs184003 0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105