Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1057519911 0.776 0.160 22 21772875 missense variant C/T snv 10
rs2239815 0.925 0.080 22 28796682 non coding transcript exon variant T/C snv 0.44 3
rs4822983 0.925 0.080 22 28719078 intron variant C/T snv 0.33 3
rs879576 1.000 0.040 22 17108356 missense variant G/A;C snv 0.11 1
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs6059655 0.790 0.080 20 34077942 intron variant A/G snv 0.95 10
rs754626
SRC
0.925 0.080 20 37388937 intron variant T/G snv 0.25 2
rs62209647 1.000 0.040 20 33917852 upstream gene variant G/C snv 4.4E-02 1
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs602662 0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 16
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs2233678 0.732 0.360 19 9834503 non coding transcript exon variant G/A;C snv 14
rs281432 0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs2233679 0.763 0.360 19 9834678 splice region variant C/T snv 0.59 11