Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10011025 1.000 0.120 4 174733072 intron variant A/C;G snv 1
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1003878 0.882 0.200 6 32332045 stop gained G/A snv 0.19 0.23 3
rs1004446 0.827 0.240 11 2148913 intron variant G/A snv 0.37 7
rs1012411 1.000 0.120 6 30364778 upstream gene variant T/G snv 0.32 1
rs1015166 0.925 0.120 6 32830954 intron variant C/G;T snv 0.28 2
rs10181656 0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs10186193 1.000 0.120 2 3550384 synonymous variant T/C snv 0.33 0.41 1
rs1020856343 0.851 0.240 5 132393705 missense variant C/T snv 4.0E-06 5
rs1022059218 0.925 0.200 2 203936863 missense variant G/A snv 2
rs1023934247 1.000 0.120 10 70598292 missense variant G/C;T snv 1
rs10255021 1.000 0.120 7 94402493 intron variant G/A snv 0.13 1
rs10272724 0.882 0.200 7 50409515 downstream gene variant T/C snv 0.24 4
rs10277986 1.000 0.120 7 50961290 intron variant T/A;C snv 1
rs10336 0.851 0.240 4 76001835 3 prime UTR variant A/G;T snv 4
rs1041740 0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs10484566 0.925 0.200 6 32867481 regulatory region variant T/G snv 6.8E-02 2
rs1048990 0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 8
rs10492166 1.000 0.120 12 9733403 upstream gene variant G/A snv 0.50 1
rs1050152 0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 10
rs10509540 0.925 0.160 10 88263276 upstream gene variant T/C snv 0.25 2
rs10517086 0.882 0.160 4 26083889 intron variant G/A snv 0.27 4
rs1052486 0.851 0.200 6 31642909 missense variant A/G snv 0.51 0.44 4