| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2167270 | 0.724 | 0.280 | 7 | 128241296 | 5 prime UTR variant | G/A | snv | 0.37 | 17 | ||
| rs34104384 | 0.851 | 0.200 | 7 | 128241254 | upstream gene variant | A/T | snv | 8.2E-03 | 5 | ||
| rs200487063 | 0.851 | 0.200 | 7 | 128241246 | upstream gene variant | G/A | snv | 2.1E-05 | 5 | ||
| rs2071045 | 0.925 | 0.120 | 7 | 128252927 | intron variant | T/C | snv | 0.18 | 3 | ||
| rs1800564 | 1.000 | 0.080 | 7 | 128254587 | missense variant | G/A;T | snv | 1.5E-04; 4.0E-06 | 1 | ||
| rs3828942 | 7 | 128254252 | intron variant | G/A | snv | 0.37 | 1 | ||||
| rs13228377 | 1.000 | 0.080 | 7 | 128239891 | upstream gene variant | A/C;G | snv | 1 | |||
| rs4731426 | 1.000 | 0.080 | 7 | 128242017 | intron variant | G/A;C;T | snv | 1 | |||
| rs200343690 | 1.000 | 0.080 | 7 | 128254653 | missense variant | G/C | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs760165439 | 1.000 | 0.080 | 7 | 128252062 | missense variant | A/G | snv | 8.0E-06 | 1 | ||
| rs724159998 | 0.882 | 0.080 | 7 | 128254557 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
| rs28954113 | 1.000 | 0.080 | 7 | 128254568 | missense variant | C/A;T | snv | 2.0E-05; 1.8E-03 | 1 | ||
| rs199647957 | 1.000 | 0.080 | 7 | 128254433 | synonymous variant | C/G;T | snv | 8.0E-06; 2.8E-05 | 1 |