Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 14
rs880315 0.925 0.120 1 10736809 intron variant T/C snv 0.32 9