Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs280519 | 0.752 | 0.320 | 19 | 10362257 | splice region variant | A/C;G | snv | 0.50 | 2 | ||
rs616488 | 0.925 | 0.080 | 1 | 10506158 | intron variant | A/G | snv | 0.27 | 1 | ||
rs7679673 | 0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 | 2 | ||
rs9790517 | 0.925 | 0.080 | 4 | 105163621 | intron variant | C/T | snv | 0.20 | 1 | ||
rs10759243 | 0.925 | 0.080 | 9 | 107543834 | upstream gene variant | C/A;T | snv | 1 | |||
rs865686 | 0.851 | 0.080 | 9 | 108126198 | regulatory region variant | G/A;T | snv | 1 | |||
rs624366 | 0.827 | 0.120 | 11 | 108283370 | intron variant | G/C | snv | 0.52 | 1 | ||
rs1801516 | 0.627 | 0.400 | 11 | 108304735 | missense variant | G/A | snv | 0.11 | 0.11 | 1 | |
rs11212617 | 0.827 | 0.200 | 11 | 108412434 | intron variant | C/A | snv | 0.49 | 1 | ||
rs2301241 | 0.827 | 0.160 | 9 | 110257228 | upstream gene variant | G/A;T | snv | 1 | |||
rs3806933 | 0.807 | 0.360 | 5 | 111071044 | 5 prime UTR variant | C/A;T | snv | 0.40 | 1 | ||
rs3204953 | 0.882 | 0.160 | 6 | 111307423 | missense variant | C/T | snv | 0.10 | 0.10 | 1 | |
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 24 | ||
rs7086803 | 0.763 | 0.160 | 10 | 112738717 | intron variant | G/A | snv | 0.20 | 1 | ||
rs11196172 | 0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 | 1 | ||
rs11196174 | 1.000 | 0.080 | 10 | 112974337 | intron variant | A/C;G | snv | 1 | |||
rs11196175 | 0.925 | 0.160 | 10 | 112976855 | intron variant | T/C | snv | 0.20 | 1 | ||
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 8 | |||
rs7904519 | 0.763 | 0.240 | 10 | 113014168 | intron variant | A/G | snv | 0.55 | 2 | ||
rs7900150 | 0.882 | 0.160 | 10 | 113034064 | intron variant | T/A;C | snv | 0.54 | 1 | ||
rs12255372 | 0.667 | 0.480 | 10 | 113049143 | intron variant | G/A;T | snv | 3 | |||
rs11552449 | 0.925 | 0.080 | 1 | 113905767 | missense variant | C/G;T | snv | 0.22 | 0.15 | 1 | |
rs1265507 | 0.925 | 0.080 | 12 | 114430333 | regulatory region variant | A/G | snv | 0.52 | 1 | ||
rs1292011 | 0.851 | 0.080 | 12 | 115398717 | regulatory region variant | A/G | snv | 0.43 | 1 | ||
rs1801131 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 1 |