Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 4
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 2
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 13
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 5
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 15
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 4
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 2
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 2
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 2
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 2
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 2
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 1
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 21
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 1
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 3
rs1801725 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 2
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 7
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 2