Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs1409851868 0.882 0.080 3 89399325 missense variant A/G snv 6
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs3749034 0.827 0.040 2 170816965 5 prime UTR variant G/A;T snv 6
rs3803300 0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs3817190 0.851 0.080 12 121274274 missense variant T/A;G snv 0.38 6
rs4500567 0.807 0.200 12 71166082 intron variant G/A;C snv 6
rs4765905 0.827 0.040 12 2240418 intron variant G/A;C snv 6
rs707284 0.807 0.080 2 211974321 intron variant T/A;C snv 6
rs1039002 0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs1106854 0.827 0.080 2 75050887 intron variant T/C;G snv 5
rs11789399 0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs2721800 0.851 0.040 7 24652933 intron variant G/A;C;T snv 5
rs28456 0.925 0.120 11 61822009 intron variant A/C;G snv 5
rs3831455 0.827 0.080 11 113904828 5 prime UTR variant GAG/- delins 5
rs9297357 0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs10835210 0.882 0.040 11 27674363 intron variant C/A;G snv 4
rs11829119 0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs12649507 0.851 0.080 4 55514317 intron variant G/A;T snv 4
rs141252918 0.882 0.040 6 151506923 intron variant G/A;C snv 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs17211233 0.882 0.040 5 81072944 intron variant T/A;C snv 4