Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12343867 0.790 0.200 9 5074189 intron variant T/C snv 0.25 9
rs12342421 0.851 0.080 9 5065750 intron variant G/C snv 0.23 4
rs10974944 0.882 0.160 9 5070831 intron variant C/G snv 0.25 4
rs1057520016 0.851 0.080 9 5089726 missense variant C/A;T snv 4
rs10974947 0.882 0.080 9 5072846 intron variant G/A snv 0.23 3
rs10815148 0.882 0.080 9 5057284 intron variant T/A snv 0.33 3
rs10815144 0.882 0.080 9 5010192 intron variant G/A snv 0.62 3
rs12349785 0.882 0.080 9 5076613 intron variant G/C snv 0.23 3
rs4495487 0.925 0.080 9 5072798 intron variant T/C snv 0.23 3
rs1339159756 0.925 0.120 9 5078395 missense variant C/G snv 2
rs121912472 0.925 0.080 9 5073742 missense variant G/C snv 2
rs121912473 0.925 0.080 9 5070026 missense variant AA/TT mnv 2
rs12339666 0.925 0.080 9 5063296 intron variant G/T snv 0.34 2
rs7046736 0.925 0.080 9 5015732 intron variant C/A snv 0.39 2
rs3808850 0.925 0.080 9 4983311 upstream gene variant T/A;C snv 2
rs7849191 0.882 0.120 9 4988761 intron variant C/T snv 0.50 2
rs7857730 0.925 0.040 9 5084049 intron variant G/A;T snv 0.63 2
rs1057519721 0.882 0.120 9 5078360 missense variant A/G snv 2
rs1159782 1.000 0.040 9 5078117 intron variant T/C snv 0.23 1
rs923941004 1.000 0.040 9 5078334 missense variant T/C snv 1
rs1392759936 1.000 0.040 9 5054778 missense variant G/A snv 7.0E-06 1
rs1479478620 1.000 0.040 9 5126768 missense variant A/G snv 1
rs2274471 1.000 0.040 9 4985879 intron variant A/G snv 0.21 1
rs3780378 1.000 0.040 9 5112288 non coding transcript exon variant C/T snv 0.51 1
rs1346944271 1.000 0.120 9 5090497 missense variant G/A snv 1.4E-05 1