Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10165883 1.000 0.080 2 69889883 upstream gene variant C/T snv 0.59 1
rs112599895 1.000 0.080 4 110735436 intergenic variant A/G snv 1.2E-02 1
rs11264280 1.000 0.080 1 154890476 intergenic variant C/T snv 0.24 1
rs114904067 1.000 0.080 4 111683665 intergenic variant G/A;T snv 1
rs11614818 1.000 0.080 12 55662031 upstream gene variant C/T snv 0.49 1
rs117640426 1.000 0.080 12 25905670 intergenic variant T/C snv 1.1E-02 1
rs117984853 1.000 0.080 6 149077964 downstream gene variant G/T snv 6.5E-02 1
rs11846704 1.000 0.080 14 34717488 upstream gene variant C/T snv 0.35 1
rs12208899 1.000 0.080 6 133153164 downstream gene variant G/A snv 0.15 1
rs12591736 1.000 0.080 15 70161800 intergenic variant G/A;C;T snv 1
rs12664873 1.000 0.080 6 122142045 intergenic variant T/C;G snv 1
rs12810346 1.000 0.080 12 114653212 downstream gene variant C/T snv 0.11 1
rs12908004 1.000 0.080 15 80384583 intron variant A/G snv 0.17 1
rs1307274 1.000 0.080 6 34272799 intron variant T/A;G snv 1
rs13105878 1.000 0.080 4 110796991 non coding transcript exon variant C/A snv 6.5E-02 1
rs13141190 1.000 0.080 4 110807458 intergenic variant A/G snv 0.47 1
rs13191450 1.000 0.080 6 122070990 intergenic variant A/C snv 0.28 1
rs13195459 1.000 0.080 6 122082413 regulatory region variant G/A snv 0.26 1
rs13216675 1.000 0.080 6 122131183 intergenic variant T/C snv 0.23 1
rs13219206 1.000 0.080 6 122093011 intergenic variant C/T snv 0.27 1
rs138311480 1.000 0.080 4 111533139 intergenic variant C/T snv 1.8E-02 1
rs143269342 1.000 0.080 4 110733185 intergenic variant C/T snv 7.7E-03 1
rs1448817 1.000 0.080 4 110719897 intergenic variant A/G snv 0.37 1
rs146518726 1.000 0.080 1 51069367 intergenic variant G/A snv 1.8E-02 1
rs149829837 1.000 0.080 4 110859850 downstream gene variant T/A snv 4.2E-02 1