Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1050501 0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs10917661 0.882 0.160 1 161671427 stop gained C/T snv 2.8E-05 3
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs7528684 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs5743836 0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs10036748 0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
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
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs1063320 0.752 0.360 6 29830972 3 prime UTR variant C/G;T snv 12
rs1707 0.925 0.120 6 29830833 3 prime UTR variant C/T snv 0.87 2