| 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 | 13 | ||
| rs2145272 | 20 | 6645571 | intergenic variant | G/A;T | snv | 7 | |||||
| rs2283847 | 22 | 27785411 | intron variant | C/A;G;T | snv | 7 | |||||
| rs979012 | 1.000 | 0.080 | 20 | 6642727 | intergenic variant | T/C | snv | 0.67 | 5 | ||
| rs1513272 | 7 | 28160478 | intron variant | C/T | snv | 0.40 | 4 | ||||
| rs6780171 | 3 | 185785668 | intron variant | T/A | snv | 0.39 | 4 | ||||
| rs56196860 | 12 | 2799164 | missense variant | C/A | snv | 1.8E-02 | 2.0E-02 | 3 | |||
| rs11085744 | 19 | 10709291 | missense variant | C/G;T | snv | 0.53 | 2 |