Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs2516400 0.827 0.320 6 31513328 upstream gene variant G/A snv 0.32 8
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 6
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 6
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 5
rs2254556 0.851 0.280 6 31374854 intron variant T/C snv 0.85 4
rs4813003 0.882 0.160 20 46134645 downstream gene variant C/A;T snv 0.19 3
rs899162 0.882 0.160 5 135459219 downstream gene variant G/A snv 1.0E-01 3
rs12068753 1.000 0.120 1 159722747 intergenic variant T/A snv 0.15 2
rs1564267 0.925 0.160 8 11480378 non coding transcript exon variant T/A;C;G snv 2
rs2061831 0.925 0.160 8 11482373 upstream gene variant T/C snv 0.25 2
rs2517892 0.925 0.240 6 29833697 downstream gene variant T/C snv 0.39 2
rs2618444 0.925 0.160 8 11480861 intron variant A/C;T snv 2
rs2736332 0.925 0.160 8 11482456 upstream gene variant G/C;T snv 2
rs2736336 0.925 0.160 8 11484361 upstream gene variant G/A;C;T snv 2
rs2848716 0.925 0.200 6 31420190 intron variant G/A;C snv 2
rs2857151 0.925 0.160 6 32795737 intergenic variant A/C;G snv 2
rs3129860 0.925 0.240 6 32433302 intergenic variant A/G;T snv 2
rs9309308 0.925 0.160 2 24771701 downstream gene variant T/C snv 0.18 2
rs13256690 1.000 0.120 8 11481059 non coding transcript exon variant G/A;C;T snv 1
rs1531577 1.000 0.120 8 11481052 non coding transcript exon variant C/T snv 0.71 1
rs17416878 1.000 0.120 1 16120485 downstream gene variant A/G snv 0.24 1
rs2244234 1.000 0.120 8 11478958 upstream gene variant T/G snv 0.83 1
rs2254891 1.000 0.120 8 11483620 upstream gene variant G/A;C snv 1