Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 25
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 19
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 5
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 4
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 4
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 3
rs11228565 0.882 0.160 11 69211113 regulatory region variant G/A snv 0.16 3
rs1327301 0.882 0.160 X 51467205 downstream gene variant C/T snv 0.29 3
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 3
rs3123078 0.882 0.160 10 46070851 regulatory region variant G/A snv 0.55 3
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 3
rs4242384 0.882 0.160 8 127506309 regulatory region variant C/A snv 0.88 3
rs5759167 0.851 0.160 22 43104206 TF binding site variant G/T snv 0.40 3
rs5919432 0.882 0.160 X 67801708 intergenic variant C/T snv 3
rs5945572 0.882 0.160 X 51486831 downstream gene variant A/G snv 3
rs6545977 0.882 0.160 2 63074029 regulatory region variant G/A snv 0.50 3
rs7127900 0.882 0.160 11 2212344 intergenic variant A/C;G snv 3
rs10875943 0.925 0.080 12 49282227 intergenic variant T/A;C snv 2
rs10936632 0.925 0.080 3 170412314 intron variant C/A snv 0.41 2
rs11199874 0.925 0.080 10 121273005 intergenic variant G/A snv 0.23 2
rs11650494 0.925 0.080 17 49267824 intron variant G/A snv 0.12 2
rs1270884 0.925 0.080 12 114247766 intergenic variant A/G snv 0.63 2
rs13083990 0.925 0.080 3 122295719 downstream gene variant T/C snv 0.30 2