Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10519198 0.925 0.080 15 78450412 intron variant C/A;G snv 2
rs1062980 0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 6
rs11638372 0.925 0.080 15 78691217 intron variant C/A;G;T snv 0.28 5
rs12441998 0.925 0.080 15 78637030 intron variant G/A snv 0.63 3
rs12594247 0.925 0.080 15 78654291 intron variant C/T snv 0.14 3
rs12910984 0.827 0.080 15 78599285 intron variant G/A;C;T snv 4
rs1316971 0.925 0.080 15 78638168 intron variant A/G;T snv 0.62 3
rs13314271 0.925 0.080 3 189639813 intron variant T/C snv 0.45 2
rs1394371 0.925 0.080 15 78432127 intergenic variant C/T snv 0.22 4
rs17487514 0.925 0.080 15 78661443 non coding transcript exon variant C/T snv 0.19 3
rs2036534 0.827 0.080 15 78534606 3 prime UTR variant T/C snv 0.26 5
rs2256543 0.925 0.080 6 29970056 downstream gene variant T/C snv 0.59 2
rs259919 0.882 0.080 6 30057726 intron variant G/A snv 0.25 6
rs259940 0.925 0.080 6 30044157 intron variant A/G snv 0.23 2
rs2656069 0.882 0.080 15 78453365 intron variant C/G;T snv 4
rs3813565 0.851 0.080 15 78727268 splice region variant G/A;T snv 6
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 4
rs6495306 0.925 0.080 15 78573551 intron variant G/A;C snv 2
rs6495309 0.807 0.080 15 78622903 upstream gene variant C/A;T snv 5
rs6495314 0.925 0.080 15 78668187 intron variant A/C snv 0.35 4
rs8038920 0.925 0.080 15 78682203 intron variant A/G snv 0.62 3
rs938682 0.851 0.080 15 78604205 intron variant G/A snv 0.72 5
rs9387478 0.851 0.080 6 117465017 intron variant C/A;T snv 3
rs4380028 0.807 0.120 15 78818751 intron variant C/T snv 0.34 4
rs680244 0.882 0.120 15 78578946 intron variant T/C snv 0.60 2