| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
| rs555607708 | 0.667 | 0.360 | 22 | 28695869 | frameshift variant | G/- | del | 2.0E-03 | 1.8E-03 | 33 | |
| rs121913365 | 0.776 | 0.320 | 7 | 140753332 | missense variant | T/A;G | snv | 10 | |||
| rs1085308039 | 0.925 | 0.080 | 10 | 87933075 | stop gained | G/T | snv | 6 | |||
| rs3735656 | 1.000 | 0.040 | 7 | 1541285 | 3 prime UTR variant | C/G;T | snv | 5 | |||
| rs10226620 | 1.000 | 0.040 | 7 | 1541881 | 3 prime UTR variant | T/C | snv | 0.69 | 4 | ||
| rs10969913 | 1.000 | 0.080 | 9 | 30866810 | intergenic variant | A/G | snv | 6.3E-02 | 3 | ||
| rs11122573 | 1.000 | 0.080 | 1 | 230701434 | upstream gene variant | C/T | snv | 8.0E-02 | 3 | ||
| rs17055178 | 1.000 | 0.080 | 5 | 157976402 | downstream gene variant | A/G | snv | 7.2E-02 | 3 | ||
| rs121913371 | 1.000 | 0.040 | 7 | 140781678 | missense variant | G/A;T | snv | 4.0E-06; 8.0E-06 | 3 | ||
| rs17630638 | 11 | 93062046 | intergenic variant | C/T | snv | 0.22 | 1 | ||||
| rs7120482 | 11 | 93058934 | regulatory region variant | G/A;T | snv | 1 |