| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs113798404 | 0.925 | 0.080 | 9 | 21970995 | missense variant | C/G;T | snv | 2 | |||
| rs11552822 | 1.000 | 9 | 21971109 | missense variant | C/A;T | snv | 4.3E-06 | 2 | |||
| rs1064794292 | 0.882 | 0.200 | 9 | 21974760 | missense variant | C/T | snv | 2 | |||
| rs104894094 | 0.763 | 0.200 | 9 | 21971058 | missense variant | C/A;G;T | snv | 8.5E-06; 4.3E-06 | 2 | ||
| rs760065045 | 1.000 | 0.080 | 9 | 21974770 | missense variant | C/A;G | snv | 4.3E-06 | 1 | ||
| rs199907548 | 0.882 | 0.160 | 9 | 21974682 | missense variant | A/C;G | snv | 6.3E-04 | 1 | ||
| rs754806883 | 0.925 | 0.160 | 9 | 21971063 | missense variant | C/A;G;T | snv | 4.3E-06; 8.5E-06 | 1 | ||
| rs757497674 | 1.000 | 0.080 | 9 | 21970958 | missense variant | G/A | snv | 4.1E-06 | 1 | ||
| rs121913386 | 0.807 | 0.120 | 9 | 21971018 | missense variant | G/A;T | snv | 1 | |||
| rs6413464 | 1.000 | 0.040 | 9 | 21970980 | missense variant | C/A;G | snv | 1.3E-03; 4.1E-06 | 1 | ||
| rs116150891 | 1.000 | 0.040 | 9 | 21970929 | missense variant | G/A;C | snv | 5.6E-04 | 2.6E-03 | 1 | |
| rs747621669 | 9 | 21970988 | missense variant | C/T | snv | 4.1E-06 | 1 | ||||
| rs6413463 | 1.000 | 0.040 | 9 | 21970990 | missense variant | A/G;T | snv | 2.9E-05; 3.0E-04 | 1 | ||
| rs36204594 | 1.000 | 0.040 | 9 | 21971180 | missense variant | G/A;T | snv | 1 | |||
| rs121913381 | 9 | 21971037 | missense variant | C/A;T | snv | 1 | |||||
| rs121913385 | 0.763 | 0.240 | 9 | 21971112 | missense variant | G/A;C | snv | 1 | |||
| rs372266620 | 0.925 | 0.120 | 9 | 21971189 | missense variant | G/A;C;T | snv | 9.1E-05; 2.3E-05; 9.1E-06 | 1 | ||
| rs104894095 | 0.827 | 0.120 | 9 | 21971200 | missense variant | C/G;T | snv | 9.0E-06 | 1 | ||
| rs587778189 | 1.000 | 9 | 21974679 | missense variant | T/A;C;G | snv | 4.0E-06; 4.0E-06 | 1 | |||
| rs758389471 | 0.882 | 0.080 | 9 | 21971160 | missense variant | C/G;T | snv | 4.7E-06; 4.7E-06 | 1 | ||
| rs104894099 | 0.851 | 0.200 | 9 | 21971183 | missense variant | A/C;T | snv | 4.6E-06 | 1 | ||
| rs104894098 | 0.851 | 0.200 | 9 | 21970982 | missense variant | A/T | snv | 1 | |||
| rs760640852 | 1.000 | 9 | 21971139 | missense variant | C/A;G;T | snv | 1 | ||||
| rs878853650 | 0.925 | 0.120 | 9 | 21974733 | missense variant | A/G | snv | 1 | |||
| rs746834149 | 1.000 | 9 | 21974724 | missense variant | C/A;G;T | snv | 4.1E-06; 1.2E-05 | 1 |