Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs767910122 0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05 17
rs794728448 0.724 0.280 7 150948445 frameshift variant CT/G delins 17
rs2069718 0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs1318358361 0.724 0.240 6 156778678 missense variant C/G snv 2.1E-05 13
rs2069727 0.763 0.320 12 68154443 intron variant T/A;C snv 9
rs794728708 0.827 0.120 1 237377386 missense variant G/A;T snv 8
rs10494366 0.851 0.200 1 162115895 intron variant G/T snv 0.54 7
rs2075575 0.851 0.200 18 26866562 intron variant G/A snv 0.31 5
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
rs786205867 0.882 0.080 1 111787039 missense variant C/T snv 3
rs1064795287 0.925 0.120 7 150947683 frameshift variant GG/T delins 2
rs12133079 1.000 0.040 1 160046674 intron variant C/A snv 0.13 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
rs1893154 0.925 0.080 18 905124 5 prime UTR variant A/G snv 0.72 2
rs199473014 0.925 0.120 7 150947684 missense variant G/T snv 2.1E-05 2
rs72466451 0.925 0.160 2 197498763 missense variant T/C snv 2
rs10081254 1.000 0.040 7 31082056 intron variant C/T snv 0.12 1
rs1178561476 1.000 0.040 1 111777204 missense variant A/G snv 1
rs1186688 1.000 0.040 1 160055093 intron variant T/C snv 0.41 1
rs17375748 1.000 0.040 1 160040361 3 prime UTR variant C/G;T snv 1