| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs143384 | 0.827 | 0.200 | 20 | 35437976 | 5 prime UTR variant | G/A | snv | 0.44 | 17 | ||
| rs5742915 | 0.925 | 0.080 | 15 | 74044292 | missense variant | T/C;G | snv | 0.35; 4.0E-06 | 7 | ||
| rs724016 | 1.000 | 0.040 | 3 | 141386728 | 5 prime UTR variant | A/G | snv | 0.52 | 5 | ||
| rs4800148 | 18 | 23144364 | intron variant | G/A;C | snv | 4 | |||||
| rs16942341 | 15 | 88845674 | synonymous variant | C/T | snv | 3.8E-02 | 6.4E-02 | 3 | |||
| rs3814333 | 1 | 184037985 | upstream gene variant | C/T | snv | 0.29 | 3 |