| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2095388 | 1.000 | 0.040 | 10 | 13142045 | upstream gene variant | A/G;T | snv | 1 | |||
| rs565070 | 1.000 | 0.040 | 9 | 35054589 | downstream gene variant | G/A | snv | 0.48 | 1 | ||
| rs62620995 | 1.000 | 0.040 | 8 | 104355036 | missense variant | C/T | snv | 8.7E-03 | 9.3E-03 | 1 | |
| rs748620045 | 1.000 | 0.040 | 14 | 61738213 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs755428183 | 1.000 | 0.040 | 18 | 79410438 | missense variant | G/A;C;T | snv | 3.6E-04 | 1 | ||
| rs916427840 | 1.000 | 0.040 | 18 | 79486424 | missense variant | C/G;T | snv | 8.0E-06 | 1 | ||
| rs756455214 | 1.000 | 0.040 | 2 | 177231420 | missense variant | T/A | snv | 4.0E-06 | 1 | ||
| rs2234968 | 1.000 | 0.040 | 10 | 13109224 | synonymous variant | G/A;C | snv | 0.24; 4.0E-06 | 1 | ||
| rs149268042 | 1.000 | 0.040 | 10 | 52315038 | missense variant | G/T | snv | 2.9E-03 | 2.6E-03 | 1 | |
| rs202119215 | 1.000 | 0.040 | 5 | 179833104 | missense variant | C/A;T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs767512628 | 1.000 | 0.040 | 5 | 179824019 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs774512680 | 1.000 | 0.040 | 5 | 179833662 | missense variant | T/A | snv | 4.0E-06 | 1 | ||
| rs776303544 | 1.000 | 0.040 | 5 | 179833707 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
| rs1162100771 | 1.000 | 0.040 | 13 | 42581288 | missense variant | C/G | snv | 1 | |||
| rs17152980 | 1.000 | 0.040 | 10 | 13234751 | upstream gene variant | G/C | snv | 9.6E-02 | 1 | ||
| rs10494112 | 0.925 | 0.080 | 1 | 109809855 | downstream gene variant | A/G | snv | 0.17 | 2 | ||
| rs2957128 | 0.925 | 0.080 | 18 | 62393502 | downstream gene variant | A/G | snv | 0.56 | 2 | ||
| rs2980996 | 0.925 | 0.080 | 18 | 62311902 | downstream gene variant | C/G;T | snv | 2 | |||
| rs499345 | 0.925 | 0.080 | 1 | 109819060 | intergenic variant | C/A | snv | 0.32 | 2 | ||
| rs2458413 | 0.925 | 0.080 | 8 | 104347204 | intron variant | C/T | snv | 0.44 | 2 | ||
| rs4294134 | 0.925 | 0.080 | 7 | 135608380 | intron variant | A/G | snv | 0.76 | 2 | ||
| rs1561570 | 0.925 | 0.080 | 10 | 13113726 | intron variant | T/C | snv | 0.43 | 2 | ||
| rs825411 | 0.925 | 0.080 | 10 | 13127374 | intron variant | A/G;T | snv | 2 | |||
| rs4941107 | 0.925 | 0.080 | 18 | 62084098 | intron variant | A/G | snv | 0.58 | 2 | ||
| rs663354 | 0.925 | 0.080 | 18 | 62087057 | intron variant | C/T | snv | 0.25 | 2 |