Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs142000963 | 0.807 | 0.240 | 1 | 156138719 | missense variant | C/A;T | snv | 1.2E-03 | 8 | ||
| rs60662302 | 0.882 | 0.200 | 1 | 156138593 | missense variant | G/A | snv | 2.1E-04 | 7.7E-04 | 5 | |
| rs61094188 | 0.925 | 0.160 | 1 | 156136257 | missense variant | C/A;T | snv | 7.6E-05 | 2 | ||
| rs61578124 | 1.000 | 0.120 | 1 | 156114992 | missense variant | G/C;T | snv | 5.4E-05 | 1 | ||
| rs57520892 | 0.776 | 0.200 | 1 | 156137204 | missense variant | G/A;C | snv | 4.1E-05 | 8 | ||
| rs61177390 | 1.000 | 0.120 | 1 | 156135992 | missense variant | G/A | snv | 3.6E-05 | 2.8E-05 | 1 | |
| rs58105277 | 1.000 | 0.120 | 1 | 156135971 | missense variant | G/A | snv | 2.8E-05 | 1 | ||
| rs13768 | 1.000 | 0.120 | 1 | 156138660 | missense variant | G/A;T | snv | 2.4E-05 | 1 | ||
| rs60695352 | 0.925 | 0.120 | 1 | 156115067 | splice donor variant | G/A;C;T | snv | 9.5E-06 | 2 | ||
| rs57629361 | 0.827 | 0.280 | 1 | 156137207 | missense variant | C/A;G;T | snv | 9.3E-06 | 5 | ||
| rs267607642 | 1.000 | 0.120 | 1 | 156136921 | missense variant | G/T | snv | 8.0E-06 | 1 | ||
| rs386134243 | 0.708 | 0.360 | 1 | 156135967 | missense variant | C/A;T | snv | 4.0E-06 | 16 | ||
| rs60864230 | 0.790 | 0.280 | 1 | 156130658 | missense variant | G/A;C;T | snv | 4.0E-06 | 7 | ||
| rs58048078 | 0.925 | 0.120 | 1 | 156134942 | stop gained | T/A;C | snv | 4.0E-06 | 2 | ||
| rs11575937 | 0.653 | 0.480 | 1 | 156136985 | missense variant | G/A;T | snv | 29 | |||
| rs60682848 | 0.790 | 0.200 | 1 | 156134838 | stop gained | C/T | snv | 7.0E-06 | 11 | ||
| rs61672878 | 0.776 | 0.200 | 1 | 156136094 | missense variant | G/A;T | snv | 11 | |||
| rs58034145 | 0.827 | 0.160 | 1 | 156134830 | missense variant | A/C | snv | 10 | |||
| rs58932704 | 0.776 | 0.200 | 1 | 156136413 | missense variant | C/T | snv | 8 | |||
| rs56984562 | 0.827 | 0.200 | 1 | 156137666 | missense variant | C/A;G;T | snv | 6 | |||
| rs57983345 | 0.851 | 0.160 | 1 | 156115034 | missense variant | A/G | snv | 6 | |||
| rs61195471 | 0.827 | 0.160 | 1 | 156134496 | missense variant | G/A | snv | 6 | |||
| rs878853220 | 0.827 | 0.200 | 1 | 156130818 | intron variant | T/G | snv | 6 | |||
| rs59332535 | 0.827 | 0.160 | 1 | 156134911 | missense variant | G/A | snv | 5 | |||
| rs60458016 | 0.827 | 0.120 | 1 | 156136036 | stop gained | G/A;T | snv | 5 |