Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs12794714 0.708 0.360 11 14892029 synonymous variant G/A snv 0.41 0.35 15
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs1131498 0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs17300539 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs1048990 0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 8