| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1182 | 0.790 | 0.160 | 9 | 129813781 | 3 prime UTR variant | C/A | snv | 0.17 | 9 | ||
| rs587776983 | 0.807 | 0.240 | 19 | 6502209 | missense variant | G/A;C;T | snv | 9 | |||
| rs11655081 | 0.851 | 0.080 | 17 | 68386068 | intron variant | T/C | snv | 0.18 | 7 | ||
| rs1801968 | 0.827 | 0.040 | 9 | 129818622 | missense variant | C/G;T | snv | 0.13; 4.0E-06 | 7 | ||
| rs587777074 | 0.790 | 0.240 | 19 | 6495688 | missense variant | C/T | snv | 4.0E-06 | 7 | ||
| rs3842225 | 0.882 | 0.120 | 9 | 129813148 | 3 prime UTR variant | C/- | del | 0.16 | 6 | ||
| rs1265889947 | 1.000 | 0.040 | 2 | 178450382 | missense variant | C/G | snv | 7.0E-06 | 1 | ||
| rs767114942 | 1.000 | 0.040 | 9 | 129818826 | missense variant | A/G | snv | 1.2E-05 | 1.4E-05 | 1 | |
| rs886041099 | 1.000 | 0.040 | 9 | 129818784 | missense variant | T/A | snv | 1 |