| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267602852 | 0.827 | 0.160 | 11 | 32417631 | missense variant | G/A | snv | 7 | |||
| rs386833945 | 0.882 | 0.080 | 19 | 35850987 | missense variant | G/A | snv | 4 | |||
| rs121912491 | 0.882 | 0.240 | 3 | 49131128 | missense variant | C/T | snv | 7.0E-06 | 4 | ||
| rs386833895 | 0.925 | 0.080 | 19 | 35845430 | missense variant | C/A | snv | 3.6E-05 | 7.0E-05 | 2 | |
| rs763972372 | 0.925 | 0.080 | 19 | 35849060 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 2 | |
| rs962888148 | 1.000 | 0.080 | 19 | 35848313 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
| rs778552202 | 1.000 | 0.080 | 19 | 35849643 | missense variant | G/A | snv | 3.6E-05 | 7.0E-06 | 1 | |
| rs1187796947 | 1.000 | 0.080 | 1 | 179564784 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs200419008 | 1.000 | 0.080 | 10 | 94252352 | missense variant | G/A;T | snv | 2.0E-05; 3.7E-04 | 1 |