Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2075184 | 0.724 | 0.240 | 2 | 102464132 | intergenic variant | T/C | snv | 0.78 | 14 | ||
rs62131887 | 0.724 | 0.240 | 19 | 10476920 | intergenic variant | C/T | snv | 0.37 | 14 | ||
rs11839053 | 0.724 | 0.240 | 13 | 106410694 | intergenic variant | T/C | snv | 7.0E-02 | 14 | ||
rs7537605 | 0.882 | 0.120 | 1 | 107800465 | intron variant | G/A;T | snv | 3 | |||
rs2153977 | 0.807 | 0.240 | 1 | 113537449 | intron variant | C/T | snv | 0.28 | 2 | ||
rs6679677 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 25 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 34 | |
rs2358994 | 0.925 | 0.120 | 1 | 113886839 | intron variant | G/A | snv | 0.16 | 2 | ||
rs4246905 | 0.716 | 0.400 | 9 | 114790969 | missense variant | T/A;C | snv | 0.76 | 15 | ||
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 6 | ||
rs7679475 | 0.925 | 0.120 | 4 | 121392885 | intergenic variant | A/C;G | snv | 2 | |||
rs62324212 | 0.724 | 0.240 | 4 | 122639784 | intron variant | C/A;G | snv | 15 | |||
rs1534422 | 0.827 | 0.160 | 2 | 12500615 | intron variant | G/A | snv | 0.52 | 4 | ||
rs7042370 | 0.724 | 0.240 | 9 | 12785074 | intron variant | T/C | snv | 0.58 | 14 | ||
rs10988542 | 0.724 | 0.240 | 9 | 129894985 | intron variant | G/A;C | snv | 14 | |||
rs11741255 | 0.724 | 0.240 | 5 | 132475490 | intron variant | G/A | snv | 0.29 | 14 | ||
rs11145763 | 0.724 | 0.240 | 9 | 136369144 | intron variant | A/C;G;T | snv | 14 | |||
rs2807264 | 0.724 | 0.240 | X | 136583619 | downstream gene variant | C/A | snv | 14 | |||
rs12863738 | 0.724 | 0.240 | X | 136949968 | intron variant | C/T | snv | 0.16 | 14 | ||
rs7831697 | 0.724 | 0.240 | 8 | 137124061 | regulatory region variant | T/A;C;G | snv | 14 | |||
rs755374 | 0.724 | 0.240 | 5 | 159402286 | intron variant | C/T | snv | 0.28 | 14 | ||
rs34884278 | 0.724 | 0.240 | 1 | 172869708 | intron variant | C/T | snv | 0.63 | 14 | ||
rs7660520 | 0.724 | 0.240 | 4 | 182824168 | upstream gene variant | G/A;C | snv | 14 | |||
rs13093110 | 0.882 | 0.120 | 3 | 188407332 | intron variant | C/T | snv | 0.42 | 3 | ||
rs6689858 | 0.724 | 0.240 | 1 | 197406337 | intron variant | T/C | snv | 0.39 | 14 |