Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 7
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 7
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs17216707 20 54115823 intergenic variant T/C snv 0.17 6
rs4665987 0.925 0.120 2 27532958 upstream gene variant G/A;T snv 6
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 5
rs6127099 20 54114863 intergenic variant A/T snv 0.28 5
rs2453533 1.000 0.080 15 45349027 intergenic variant C/A snv 0.56 4
rs6465825 1.000 0.080 7 77787122 downstream gene variant T/C snv 0.41 4
rs7123489 1.000 0.080 11 65756781 intron variant C/A snv 0.29 4
rs10874312 1 82478888 intron variant G/A snv 0.70 3
rs1933182 1.000 0.080 1 109457216 intergenic variant A/C snv 0.63 3
rs2290263 7 25847658 intergenic variant G/A snv 0.77 3
rs10277115 7 1245559 regulatory region variant A/T snv 0.57 2
rs10840341 11 2095263 intergenic variant T/A;C snv 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
rs1705694 8 23912105 intergenic variant A/C;G snv 0.50 2
rs36071802 8 23858358 upstream gene variant T/A;C snv 2
rs3758086 8 23857479 upstream gene variant G/A snv 0.37 2