Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 8
rs11153730 6 118346359 intergenic variant T/C snv 0.40 4
rs12061601 1.000 0.040 1 169101212 intron variant T/C snv 0.16 3
rs12143842 0.925 0.160 1 162064100 intergenic variant C/T snv 0.22 3
rs4657139 0.925 0.120 1 162060117 intergenic variant A/T snv 0.48 3
rs12036340 1 162045950 intergenic variant A/G snv 0.24 2
rs17779747 1.000 0.040 17 70498851 regulatory region variant G/T snv 0.24 2
rs2968863 1.000 0.080 7 150926049 intergenic variant C/T snv 0.16 2
rs2968864 7 150925074 intergenic variant T/C snv 0.16 2
rs10040989 5 138238036 intergenic variant G/A snv 0.12 1
rs10775360 17 70329727 intron variant C/T snv 0.25 1
rs1106399 2 200139114 regulatory region variant A/C snv 0.15 1
rs114950282 5 3657167 intergenic variant C/T snv 1.3E-02 1
rs11970286 6 118359211 intergenic variant C/T snv 0.36 1
rs12210733 6 118331912 intergenic variant G/A;C snv 1
rs12210810 6 118332041 intergenic variant G/C;T snv 1
rs12444261 16 11640786 upstream gene variant G/T snv 0.21 1
rs12604566 18 72963471 intergenic variant C/T snv 0.71 1
rs1320997 6 17368796 intergenic variant C/A snv 1.8E-02 1
rs1380181 17 15289739 intron variant A/G snv 0.75 1
rs138682672 4 53797853 intron variant G/A snv 3.6E-03 1
rs1396515 17 70434852 intergenic variant G/C snv 0.56 1
rs1415268 1 162036661 upstream gene variant A/T snv 0.56 1
rs1439840 2 122651367 intron variant T/C snv 5.6E-02 1
rs144230162 8 71727088 regulatory region variant A/G snv 2.4E-03 1