Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4900384 0.882 0.160 14 98032614 intergenic variant A/G snv 0.40 4
rs7172432 0.925 0.080 15 62104190 intergenic variant A/G snv 0.51 4
rs7193788 0.925 0.120 16 82622555 upstream gene variant A/G snv 0.16 4
rs7910977 0.882 0.160 10 92450119 downstream gene variant C/T snv 0.17 4
rs9402571 0.882 0.080 6 134167822 downstream gene variant T/G snv 0.22 4
rs10885390 0.925 0.080 10 112881038 regulatory region variant T/A snv 0.30 3
rs10941191 1.000 0.040 5 34504693 intergenic variant C/A;T snv 3
rs11071657 1.000 0.040 15 62141763 regulatory region variant A/G snv 0.31 3
rs12363572 0.925 0.080 11 68621498 upstream gene variant C/T snv 0.10 3
rs1974990 1.000 0.040 2 169790406 non coding transcript exon variant G/T snv 0.90 3
rs200950799 1.000 0.040 12 17004185 intergenic variant C/T snv 1.1E-02 3
rs2105903 1.000 0.040 6 32427879 intergenic variant A/T snv 0.14 3
rs3132374 1.000 0.040 6 28900717 downstream gene variant C/G snv 5.3E-02 3
rs60307791 1.000 0.040 11 65767714 intron variant TT/-;T;TTT;TTTT delins 3
rs6583813 0.925 0.080 10 92450182 downstream gene variant C/A;T snv 3
rs7690819 1.000 0.040 4 111199502 intergenic variant A/G;T snv 3
rs10818684 1.000 0.040 9 122407651 intron variant C/T snv 0.62 2
rs1206634 1.000 0.040 X 96302380 intron variant T/A;G snv 2
rs1260236 1.000 0.040 9 6023030 intergenic variant A/G snv 2
rs12910524 1.000 0.040 15 101262360 intergenic variant T/A;C snv 2
rs1543654 1.000 0.040 21 34426752 upstream gene variant T/C snv 2
rs181914932 1.000 0.040 20 45932640 non coding transcript exon variant T/C snv 1.6E-02 2
rs2863389 1.000 0.040 3 166431104 intergenic variant C/T snv 0.17 2
rs4258701 1.000 0.040 18 27895834 intergenic variant C/T snv 0.28 2
rs57922 1.000 0.040 5 74282114 intron variant C/T snv 0.40 2