Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075575 0.851 0.200 18 26866562 intron variant G/A snv 0.31 5
rs199473124 0.851 0.120 3 38603902 missense variant A/T snv 8.0E-06 7.0E-06 4
rs9951307 0.882 0.120 18 26850565 intron variant G/A snv 0.65 5
rs199473604 0.882 0.120 3 38560394 missense variant G/T snv 4
rs121434278 0.882 0.120 1 75740094 missense variant G/A snv 4.0E-05 7.0E-05 3
rs137854609 0.882 0.120 3 38581170 missense variant C/A;T snv 7.9E-05 3
rs199473320 0.882 0.120 3 38550878 missense variant G/C snv 6.0E-05 4.0E-04 3
rs786205867 0.882 0.080 1 111787039 missense variant C/T snv 3
rs77931234 0.925 0.120 1 75761161 missense variant A/C;G snv 3.3E-03 3
rs1064795287 0.925 0.120 7 150947683 frameshift variant GG/T delins 2
rs1188884950 0.925 0.080 5 474952 missense variant A/G snv 4.2E-06 2
rs121909281 0.925 0.120 3 8733916 missense variant G/A;C snv 4.3E-04 2
rs121909282 0.925 0.120 3 8745647 missense variant T/G snv 1.4E-05 2
rs1361625573 0.925 0.080 5 474979 missense variant A/G snv 7.0E-06 2
rs137854610 0.925 0.120 3 38550895 missense variant C/T snv 2.8E-05 1.7E-04 2
rs149344567 0.925 0.120 1 111776247 missense variant C/T snv 6.4E-05 5.6E-05 2
rs1893154 0.925 0.080 18 905124 5 prime UTR variant A/G snv 0.72 2
rs199472728 0.925 0.120 11 2572885 missense variant A/G snv 1.8E-04 1.3E-04 2
rs199473014 0.925 0.120 7 150947684 missense variant G/T snv 2.1E-05 2
rs199473573 0.925 0.120 3 38604007 missense variant A/C snv 1.6E-05 7.0E-06 2
rs2856966 0.925 0.080 18 907709 missense variant A/G snv 0.19 0.18 2
rs72466451 0.925 0.160 2 197498763 missense variant T/C snv 2
rs72552293 0.925 0.120 3 32140231 missense variant A/G snv 2.5E-03 2.9E-03 2
rs116840776 1.000 0.040 3 8745627 missense variant C/G snv 1.4E-03 1.6E-03 2
rs12133079 1.000 0.040 1 160046674 intron variant C/A snv 0.13 2