Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2779180 1.000 0.080 19 4841139 intron variant A/G snv 0.37 1
rs4803223 1.000 0.080 19 39255579 upstream gene variant A/G snv 0.13 1
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs2287886 0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs17047200 0.827 0.200 4 166008836 intron variant A/T snv 0.18 5
rs5743704 0.763 0.240 4 153704799 missense variant C/A snv 2.8E-02 2.8E-02 9
rs4803217 0.882 0.120 19 39243580 3 prime UTR variant C/A snv 0.39 4
rs8109886 1.000 0.080 19 39252122 upstream gene variant C/A snv 0.53 1
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs4273729 0.851 0.240 6 32710820 upstream gene variant C/A;G;T snv 5
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs3921 0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8
rs28416813 1.000 0.080 19 39245004 5 prime UTR variant C/G snv 0.31 0.39 1
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs2230201
C3
0.882 0.200 19 6713280 synonymous variant C/G;T snv 0.19 3
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs2071286 0.752 0.280 6 32212119 intron variant C/T snv 0.17 12
rs2854116 0.807 0.200 11 116829453 upstream gene variant C/T snv 0.51 7
rs11854484 0.925 0.120 15 45253280 missense variant C/T snv 0.47 0.45 2