| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17663555 | 1.000 | 0.080 | 5 | 73136209 | intron variant | C/A;G;T | snv | 3 | |||
| rs566164 | 1.000 | 0.080 | 6 | 109185258 | intron variant | A/G | snv | 0.73 | 2 | ||
| rs1060915 | 1.000 | 0.080 | 17 | 43082453 | synonymous variant | A/G | snv | 0.35 | 0.30 | 1 | |
| rs1064795860 | 1.000 | 0.080 | 17 | 7675155 | missense variant | G/A | snv | 1 | |||
| rs11075884 | 1.000 | 0.080 | 16 | 71321332 | intergenic variant | A/C;G | snv | 1 | |||
| rs1186364060 | 1.000 | 0.080 | 1 | 91353084 | missense variant | C/T | snv | 1 | |||
| rs140510218 | 1.000 | 0.080 | 16 | 67621458 | synonymous variant | A/G | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs143282828 | 1.000 | 0.080 | 5 | 176968697 | missense variant | A/G | snv | 7.3E-04 | 7.3E-04 | 1 | |
| rs152451 | 1.000 | 0.080 | 16 | 23634870 | missense variant | T/A;C | snv | 0.10 | 1 | ||
| rs1801201 | 1.000 | 0.080 | 17 | 39723332 | missense variant | A/C;G | snv | 4.0E-06; 4.9E-03 | 1 | ||
| rs2241268 | 1.000 | 0.080 | 15 | 85735078 | missense variant | G/A | snv | 0.22 | 0.19 | 1 | |
| rs397509062 | 1.000 | 0.080 | 17 | 43104223 | missense variant | A/G | snv | 1 | |||
| rs45551636 | 1.000 | 0.080 | 16 | 23622972 | missense variant | C/G;T | snv | 1.6E-02 | 1 | ||
| rs4843075 | 1.000 | 0.080 | 15 | 85581324 | missense variant | G/A;C | snv | 0.61; 4.0E-06 | 1 | ||
| rs530464947 | 1.000 | 0.080 | 17 | 43092137 | missense variant | T/C | snv | 1.6E-05 | 4.2E-05 | 1 | |
| rs56343424 | 1.000 | 0.080 | 15 | 74720496 | missense variant | C/A;T | snv | 2.1E-03; 3.3E-05 | 1 | ||
| rs751942421 | 1.000 | 0.080 | 11 | 562702 | missense variant | C/T | snv | 1.4E-05 | 7.0E-06 | 1 | |
| rs753904217 | 1.000 | 0.080 | 1 | 109690557 | missense variant | G/A | snv | 1.9E-04 | 6.6E-05 | 1 | |
| rs756522395 | 1.000 | 0.080 | 11 | 108257484 | missense variant | C/G;T | snv | 1 | |||
| rs758898660 | 1.000 | 0.080 | 5 | 73892052 | missense variant | G/A | snv | 4.4E-06 | 1 | ||
| rs80357007 | 1.000 | 0.080 | 17 | 43051107 | missense variant | C/A;T | snv | 1 | |||
| rs80358505 | 1.000 | 0.080 | 13 | 32319249 | missense variant | A/G;T | snv | 1 | |||
| rs996659898 | 1.000 | 0.080 | 20 | 57500314 | missense variant | G/C | snv | 1 | |||
| rs398122697 | 0.925 | 0.080 | 17 | 43049170 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
| rs16940 | 0.882 | 0.080 | 17 | 43093220 | synonymous variant | A/G | snv | 0.35 | 0.29 | 5 |