Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1324694 | 0.925 | 0.120 | 10 | 100186688 | upstream gene variant | C/T | snv | 7.8E-02 | 2 | ||
rs1800977 | 0.851 | 0.240 | 9 | 104928169 | intron variant | G/A;C | snv | 5 | |||
rs619203 | 0.851 | 0.160 | 6 | 117301021 | missense variant | G/C | snv | 0.20 | 0.19 | 6 | |
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs10986769 | 0.925 | 0.120 | 9 | 125460061 | intron variant | A/G;T | snv | 2 | |||
rs12679196 | 0.925 | 0.120 | 8 | 139800104 | intron variant | C/T | snv | 0.13 | 2 | ||
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs3027898 | 0.752 | 0.360 | X | 154010439 | downstream gene variant | C/A | snv | 11 | |||
rs1059703 | 0.851 | 0.280 | X | 154013378 | missense variant | G/A | snv | 0.67 | 6 | ||
rs3111754 | 1.000 | 0.120 | 2 | 230868988 | intron variant | T/C | snv | 0.43 | 1 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs121918097 | 0.790 | 0.280 | 18 | 31595137 | missense variant | G/A | snv | 10 | |||
rs73933023 | 1.000 | 0.120 | 19 | 38566975 | missense variant | C/G;T | snv | 2.1E-03 | 1 | ||
rs3918242 | 0.602 | 0.680 | 20 | 46007337 | upstream gene variant | C/T | snv | 0.14 | 54 | ||
rs17576 | 0.557 | 0.760 | 20 | 46011586 | missense variant | A/G | snv | 0.39 | 0.36 | 73 | |
rs17577 | 0.649 | 0.520 | 20 | 46014472 | missense variant | G/A;C | snv | 0.16 | 31 | ||
rs762890408 | 0.925 | 0.120 | 21 | 46431646 | missense variant | C/T | snv | 4.0E-05 | 2.8E-05 | 2 | |
rs144757781 | 0.925 | 0.120 | 21 | 46431895 | missense variant | G/A;T | snv | 5.5E-04 | 2 | ||
rs777785946 | 1.000 | 0.120 | 11 | 46723267 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs200525645 | 1.000 | 0.120 | 11 | 46725970 | missense variant | G/A;T | snv | 2.0E-05 | 1 | ||
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
rs710968 | 0.925 | 0.120 | 7 | 74083398 | intron variant | A/G | snv | 0.75 | 2 | ||
rs16936752 | 0.925 | 0.120 | 9 | 93301408 | intron variant | T/G | snv | 8.3E-02 | 2 | ||
rs886905373 | 0.925 | 0.120 | 14 | 94614481 | missense variant | G/A | snv | 2.8E-05 | 3 |