Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 59
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 17
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 12
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 10
rs2069514 0.807 0.160 15 74745879 upstream gene variant G/A snv 0.13 9
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 9
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 8
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 8
rs132793 0.851 0.160 22 41667677 downstream gene variant A/C;G;T snv 7
rs2555639 0.851 0.080 4 174540379 non coding transcript exon variant T/C snv 0.38 7
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 7
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 6
rs2410373 0.851 0.120 8 16066997 intergenic variant A/C snv 0.34 6
rs7859384 0.882 0.120 9 79507370 intron variant A/C;G snv 6
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 6
rs9325782 0.851 0.120 8 16232964 intron variant C/T snv 0.87 6
rs2853668 0.882 0.080 5 1299910 upstream gene variant G/T snv 0.33 5
rs28714259 0.882 0.120 15 23463380 intergenic variant G/A snv 0.19 5
rs406193 0.882 0.120 20 32811837 downstream gene variant T/C snv 0.91 5
rs9600079 0.925 0.080 13 73154002 intergenic variant G/T snv 0.46 5
rs1015213 0.851 0.040 8 51974981 intron variant C/T snv 0.14 4
rs143969848 0.925 0.160 3 36958902 TF binding site variant G/A snv 9.8E-03 4