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
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 31
rs11887534 0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27
rs3740066 0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs2266788 0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs2287622 0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 16
rs3197999 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 16
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14