Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs3802842 0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs4939827 0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs1011970 0.677 0.320 9 22062135 intron variant G/T snv 0.23 22
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs2854744 0.695 0.520 7 45921476 intron variant G/T snv 0.48 20
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs11200014 0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 19
rs4696480 0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs597808 0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs11196172 0.708 0.200 10 112967084 intron variant G/A snv 0.13 18
rs12953717 0.724 0.240 18 48927559 intron variant C/T snv 0.36 18
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs174533 0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 18