Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11228565 0.882 0.160 11 69211113 regulatory region variant G/A snv 0.16 3
rs1154865 0.882 0.160 12 73596057 intergenic variant C/G snv 0.22 3
rs1327301 0.882 0.160 X 51467205 downstream gene variant C/T snv 0.29 3
rs16886165 0.882 0.160 5 56727256 intergenic variant T/C;G snv 0.22 3
rs3123078 0.882 0.160 10 46070851 regulatory region variant G/A snv 0.55 3
rs4242384 0.882 0.160 8 127506309 regulatory region variant C/A snv 0.88 3
rs4699052 0.925 0.200 4 103216633 intergenic variant C/T snv 0.44 3
rs5945572 0.882 0.160 X 51486831 downstream gene variant A/G snv 3
rs6545977 0.882 0.160 2 63074029 regulatory region variant G/A snv 0.50 3
rs7127900 0.882 0.160 11 2212344 intergenic variant A/C;G snv 3
rs9543325 0.882 0.200 13 73342491 regulatory region variant C/G;T snv 3
rs1572072 1.000 0.120 13 23553071 intergenic variant G/T snv 0.36 2
rs28421666 1.000 0.120 6 32624960 upstream gene variant A/G snv 6.9E-02 2
rs3129055 1.000 0.120 6 29702484 regulatory region variant A/G snv 0.24 2
rs7169431 0.925 0.200 15 56048698 intergenic variant A/G;T snv 2
rs1610588 1.000 0.120 6 29708939 upstream gene variant C/T snv 0.19 1
rs1610742 1.000 0.120 6 29710175 upstream gene variant T/C snv 0.19 1
rs232228 1.000 0.120 2 88859459 intron variant G/A snv 0.15 1
rs2735845 1.000 0.120 5 1300469 intergenic variant C/G snv 0.16 1
rs29218 1.000 0.120 6 29639652 upstream gene variant A/G snv 0.17 1
rs3095267 1.000 0.120 6 29639269 upstream gene variant G/C;T snv 1
rs3095341 1.000 0.120 6 30758971 intron variant T/C snv 0.69 1
rs3131866 1.000 0.120 6 29703963 downstream gene variant G/A snv 0.24 1
rs533550179 1.000 0.120 6 29714462 intergenic variant C/T snv 1
rs577078190 1.000 0.120 6 29716031 intergenic variant G/A snv 1