Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001007 0.827 0.120 3 46387167 intron variant A/G;T snv 5
rs1004234 0.827 0.120 5 132421409 intron variant A/G;T snv 5
rs10510607 0.827 0.120 3 28244770 intron variant C/T snv 0.15 5
rs10761648 0.827 0.120 10 62594503 intron variant C/T snv 0.20 5
rs10775412 0.827 0.120 17 27542007 intron variant A/C snv 0.30 5
rs10870077 0.827 0.120 9 136369439 intron variant C/G snv 0.38 5
rs10889676 0.827 0.120 1 67256884 intron variant C/A;T snv 5
rs10988542 0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11098964 0.827 0.120 4 79966815 intron variant A/G;T snv 5
rs11117431 0.807 0.160 16 85981710 intron variant A/G snv 0.18 6
rs111305875 0.827 0.120 6 167098098 intron variant T/G snv 3.0E-02 5
rs11145763 0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs11168249 0.807 0.120 12 47814585 intron variant T/C snv 0.50 8
rs11221322 0.827 0.120 11 128476898 intron variant T/C snv 0.13 5
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs11229555 0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs114202211 0.827 0.120 1 113943285 intron variant T/C snv 8.1E-03 5
rs114846446 0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs11580078 0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs116046827
BSN
0.827 0.120 3 49618715 intron variant T/C snv 8.6E-03 5
rs11614178 0.827 0.120 12 68114342 intron variant G/A;T snv 0.26 6
rs11624293 0.827 0.120 14 88022477 intron variant T/C snv 0.13 5
rs11675538 0.827 0.120 2 65459327 intron variant C/T snv 0.29 5
rs11691685 0.827 0.120 2 144724260 intron variant A/G snv 5.2E-02 5
rs11741255 0.724 0.240 5 132475490 intron variant G/A snv 0.29 14