Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs406193 0.882 0.120 20 32811837 downstream gene variant T/C snv 0.91 5
rs9600079 0.925 0.080 13 73154002 intergenic variant G/T snv 0.46 5
rs11536858 0.851 0.240 9 117701869 upstream gene variant G/A;T snv 4
rs13083990 0.925 0.080 3 122295719 downstream gene variant T/C snv 0.30 4
rs565453 0.882 0.160 5 112849696 intron variant A/C;G snv 4
rs5759167 0.851 0.160 22 43104206 TF binding site variant G/T snv 0.40 4
rs6983269 0.925 0.080 8 2741967 intron variant C/A;G;T snv 0.42 4
rs10969913 1.000 0.080 9 30866810 intergenic variant A/G snv 6.3E-02 3
rs11067228 0.925 0.080 12 114656455 downstream gene variant A/G snv 0.37 3
rs11122573 1.000 0.080 1 230701434 upstream gene variant C/T snv 8.0E-02 3
rs11228565 0.882 0.160 11 69211113 regulatory region variant G/A snv 0.16 3
rs12757998 0.925 0.080 1 182569343 downstream gene variant C/T snv 0.24 3
rs1327301 0.882 0.160 X 51467205 downstream gene variant C/T snv 0.29 3
rs17055178 1.000 0.080 5 157976402 downstream gene variant A/G snv 7.2E-02 3
rs3123078 0.882 0.160 10 46070851 regulatory region variant G/A snv 0.55 3
rs4054823 0.882 0.080 17 13721707 intergenic variant T/C snv 0.42 3
rs4242384 0.882 0.160 8 127506309 regulatory region variant C/A snv 0.88 3
rs4631830 0.925 0.080 10 46052478 upstream gene variant A/G snv 0.43 3
rs5919432 0.882 0.160 X 67801708 intergenic variant C/T snv 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
rs10749408 0.925 0.080 10 121208012 intergenic variant C/T snv 0.72 2
rs10788165 0.925 0.080 10 121284700 regulatory region variant T/G snv 0.35 2
rs10861905 0.925 0.120 12 108373556 regulatory region variant C/A snv 7.6E-02 2