| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs34670419 | 1.000 | 0.080 | 7 | 99533211 | 3 prime UTR variant | G/A;T | snv | 7.7E-06; 2.6E-02 | 7 | ||
| rs148982377 | 7 | 99477415 | intron variant | T/C | snv | 3.2E-02 | 4 | ||||
| rs10786714 | 10 | 102838849 | intron variant | G/C | snv | 0.25 | 2 | ||||
| rs112295236 | 11 | 63147874 | intron variant | C/A;G | snv | 2 | |||||
| rs139203625 | 11 | 95366701 | intergenic variant | C/T | snv | 1.1E-02 | 1 | ||||
| rs72906582 | 18 | 47696400 | intergenic variant | G/A;C | snv | 1 | |||||
| rs77032081 | 11 | 13341732 | intron variant | C/T | snv | 8.7E-03 | 1 | ||||
| rs139441768 | 5 | 91383446 | intron variant | T/C | snv | 1.0E-02 | 1 | ||||
| rs142754737 | 11 | 43844164 | intron variant | C/T | snv | 1.1E-02 | 1 | ||||
| rs79589801 | 1 | 210880719 | intron variant | C/T | snv | 1.2E-02 | 1 | ||||
| rs140935700 | 5 | 91316148 | upstream gene variant | G/A | snv | 9.4E-03 | 1 |