| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 | |
| rs11172113 | 0.882 | 0.080 | 12 | 57133500 | intron variant | T/C | snv | 0.42 | 10 | ||
| rs2869966 | 1.000 | 0.040 | 4 | 88947927 | intron variant | C/T | snv | 0.47 | 9 | ||
| rs13141641 | 1.000 | 0.040 | 4 | 144585304 | intron variant | T/C | snv | 0.32 | 8 | ||
| rs1529672 | 1.000 | 0.040 | 3 | 25479091 | intron variant | C/A;T | snv | 6 | |||
| rs11722225 | 4 | 105845273 | intron variant | T/C | snv | 5.5E-02 | 5 | ||||
| rs2798641 | 6 | 108946847 | intron variant | C/T | snv | 0.15 | 5 | ||||
| rs7753012 | 6 | 142424746 | intron variant | T/G | snv | 0.50 | 5 |