Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs585362 1 109247173 upstream gene variant C/G;T snv 4
rs611917 1.000 0.040 1 109272630 non coding transcript exon variant A/G snv 0.28 0.32 4
rs734359 1 41480231 intron variant C/T snv 7.5E-02 4
rs10788994 1 55035303 upstream gene variant C/T snv 0.20 3
rs10858082 1 109256099 intron variant G/A snv 0.48 3
rs10888898 1 55050835 intron variant A/G snv 0.59 3
rs10916704 1 20074498 intron variant G/A;T snv 3
rs11206514 1 55050331 intron variant C/A snv 0.52 3
rs11573244 1 20081089 intron variant C/T snv 6.6E-03 3
rs11577931 1 109278262 downstream gene variant A/G snv 5.5E-02 3
rs1165287 1 55054539 intron variant G/A snv 0.52 3
rs11806129 1 94016821 intron variant A/G;T snv 3
rs11806638 1 55052487 intron variant C/A;G snv 3
rs12027135 1 25449242 intron variant A/T snv 0.50 3
rs12087003 1 94037627 intron variant A/G snv 6.3E-02 3
rs12127701 1 109295642 intron variant A/G snv 6.2E-02 3
rs17035665 1 109271097 intron variant C/T snv 0.19 3
rs17111503 0.925 0.160 1 55037775 upstream gene variant A/G snv 0.22 3
rs17645031 1 109292316 downstream gene variant C/T snv 7.9E-02 3
rs17646665 1.000 0.080 1 109369429 intron variant A/G snv 5.8E-02 3
rs17646731 1 109376903 intron variant G/A snv 4.6E-02 3
rs2149041 1 55036464 upstream gene variant C/G snv 0.17 3
rs2182833 1 55034756 upstream gene variant A/G snv 0.23 3
rs2479409 1.000 0.040 1 55038977 upstream gene variant G/A snv 0.66 3
rs2479410 1 55040188 intron variant G/A snv 0.29 3