Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10941191 1.000 0.040 5 34504693 intergenic variant C/A;T snv 3
rs12428035 13 95648618 upstream gene variant C/A;T snv 3
rs1913641 0.925 0.120 8 75571004 downstream gene variant T/G snv 0.58 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
rs2290263 7 25847658 intergenic variant G/A snv 0.77 3
rs3132374 1.000 0.040 6 28900717 downstream gene variant C/G snv 5.3E-02 3
rs34861762 1.000 0.080 8 23890907 regulatory region variant C/T snv 0.37 3
rs60307791 1.000 0.040 11 65767714 intron variant TT/-;T;TTT;TTTT delins 3
rs7012637 8 9315699 intron variant G/A;C snv 3
rs10277115 7 1245559 regulatory region variant A/T snv 0.57 2
rs10840341 11 2095263 intergenic variant T/A;C snv 2
rs115114609 1.000 0.080 5 88448197 intron variant G/A snv 3.4E-02 2
rs11604462 11 65784177 upstream gene variant G/A snv 0.30 2
rs11742501 5 151727535 upstream gene variant T/C snv 0.29 2
rs12458009 18 61683274 intron variant T/C;G snv 2
rs12845465 X 8944553 intergenic variant T/C snv 1.5E-03 2
rs143297173 6 55418058 intergenic variant A/C snv 6.7E-04 2
rs1705694 8 23912105 intergenic variant A/C;G snv 0.50 2
rs1813937 1.000 0.080 11 50509630 intergenic variant C/T snv 0.76 2
rs281380 19 48711213 downstream gene variant T/C snv 0.39 2
rs35320690 3 136213652 intergenic variant T/C snv 0.20 2
rs36071802 8 23858358 upstream gene variant T/A;C snv 2
rs3758086 8 23857479 upstream gene variant G/A snv 0.37 2