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 | |||
rs10094579 | 0.807 | 0.280 | 8 | 89837077 | downstream gene variant | C/A | snv | 0.18 | 5 | ||
rs10510607 | 0.827 | 0.120 | 3 | 28244770 | intron variant | C/T | snv | 0.15 | 5 | ||
rs10743181 | 0.827 | 0.120 | 11 | 2208529 | regulatory region variant | A/G | snv | 0.77 | 5 | ||
rs10748781 | 0.763 | 0.160 | 10 | 99523573 | upstream gene variant | C/A;G | snv | 11 | |||
rs10750899 | 0.827 | 0.120 | 11 | 58517478 | intergenic variant | G/A | snv | 0.95 | 5 | ||
rs10758669 | 0.763 | 0.280 | 9 | 4981602 | upstream gene variant | C/A;T | snv | 6 | |||
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 | ||
rs10800314 | 0.827 | 0.120 | 1 | 161502999 | upstream gene variant | C/A | snv | 0.65 | 5 | ||
rs10822050 | 0.724 | 0.240 | 10 | 62679011 | downstream gene variant | T/C | snv | 0.33 | 14 | ||
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 | |||
rs10995271 | 0.776 | 0.280 | 10 | 62678726 | downstream gene variant | G/C | snv | 0.32 | 5 | ||
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 | ||
rs11190133 | 0.827 | 0.120 | 10 | 99518968 | intergenic variant | C/T | snv | 0.26 | 5 | ||
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 |