Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs1263173 0.925 0.080 11 116810292 downstream gene variant G/A snv 0.53 4
rs174546 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs174570 0.882 0.200 11 61829740 intron variant C/T snv 0.15 11
rs2075291 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs6589566 0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs7115242 0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs7120118 0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs10846744 0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12369179 0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs4905014 0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs10468017 0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs147233090 0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs1532085 0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20