| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1805017 | 0.851 | 0.240 | 6 | 46716485 | missense variant | C/A;T | snv | 4.0E-06; 0.31 | 5 | ||
| rs2071746 | 0.708 | 0.320 | 22 | 35380679 | intron variant | A/T | snv | 0.49 | 18 | ||
| rs213950 | 0.716 | 0.320 | 7 | 117559479 | missense variant | G/A | snv | 0.47 | 0.57 | 16 | |
| rs267606982 | 0.742 | 0.120 | 7 | 142751938 | missense variant | GC/AT | mnv | 11 | |||
| rs371282890 | 0.827 | 0.120 | 8 | 19955900 | missense variant | C/G | snv | 1.1E-04 | 6.3E-05 | 6 | |
| rs4073 | 0.566 | 0.800 | 4 | 73740307 | upstream gene variant | A/T | snv | 0.46 | 64 | ||
| rs4251961 | 0.763 | 0.200 | 2 | 113116890 | intron variant | T/C | snv | 0.29 | 10 | ||
| rs497078 | 0.925 | 0.040 | 1 | 15440540 | synonymous variant | C/A;T | snv | 3.7E-03; 9.1E-02 | 2 | ||
| rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
| rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
| rs5029924 | 0.851 | 0.200 | 6 | 137866361 | intron variant | C/T | snv | 0.13 | 4 | ||
| rs5275 | 0.583 | 0.560 | 1 | 186673926 | 3 prime UTR variant | A/G;T | snv | 55 | |||
| rs5707 | 1.000 | 0.040 | 1 | 204160543 | intron variant | A/C;G;T | snv | 0.25; 2.0E-05; 1.2E-05 | 2 | ||
| rs5743795 | 1.000 | 0.040 | 4 | 38830874 | intron variant | C/T | snv | 0.14 | 1 | ||
| rs61734659 | 0.790 | 0.160 | 7 | 142774035 | missense variant | G/A | snv | 1.4E-02 | 8 | ||
| rs7057398 | 0.827 | 0.080 | X | 106901299 | intron variant | T/C | snv | 0.41 | 5 | ||
| rs748405415 | 0.790 | 0.160 | 7 | 142773993 | stop gained | G/A;T | snv | 8 | |||
| rs752688735 | 0.925 | 0.040 | 7 | 142752547 | missense variant | G/A | snv | 2 | |||
| rs756271986 | 0.925 | 0.040 | 7 | 142773430 | missense variant | GC/AT | mnv | 2 | |||
| rs764176833 | 0.925 | 0.040 | 7 | 142773430 | missense variant | G/A | snv | 2 | |||
| rs76863441 | 0.672 | 0.440 | 6 | 46709361 | missense variant | C/A | snv | 4.5E-03 | 1.3E-03 | 25 | |
| rs773891125 | 0.827 | 0.120 | 8 | 19955896 | frameshift variant | CT/- | delins | 6 | |||
| rs777418530 | 0.763 | 0.120 | 16 | 84845883 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 10 | |
| rs778574118 | 1.000 | 0.040 | 10 | 113721138 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs78655421 | 0.716 | 0.240 | 7 | 117530975 | missense variant | G/A;C;T | snv | 1.5E-03; 1.2E-05 | 18 |