Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs2287622 0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs368234815 0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs10877012 0.763 0.280 12 57768302 intron variant G/C;T snv 10
rs10814325 0.827 0.200 9 36036597 upstream gene variant T/A;C;G snv 7
rs2854117 0.851 0.200 11 116829426 upstream gene variant T/A;C snv 6
rs4273729 0.851 0.240 6 32710820 upstream gene variant C/A;G;T snv 5
rs758564400
REN
0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06 5
rs8878 0.827 0.280 4 76021147 3 prime UTR variant A/C;G snv 5
rs2267716 0.851 0.120 7 30677027 intron variant T/A;C snv 4
rs2230201
C3
0.882 0.200 19 6713280 synonymous variant C/G;T snv 0.19 3
rs12989760 0.925 0.120 2 250470 intron variant T/C snv 2
rs12952093 1.000 0.080 17 78367559 intron variant A/C;T snv 1
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1470452230 0.925 0.120 9 135561895 missense variant A/C snv 7.0E-06 2
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs5743704 0.763 0.240 4 153704799 missense variant C/A snv 2.8E-02 2.8E-02 9
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42