| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs111511318 | 1.000 | 0.080 | 5 | 156998817 | intergenic variant | C/A | snv | 2.9E-02 | 1 | ||
| rs116399066 | 1.000 | 0.080 | 1 | 143723149 | upstream gene variant | C/A;T | snv | 1 | |||
| rs1979860 | 1.000 | 0.080 | 5 | 174586529 | regulatory region variant | C/T | snv | 1.8E-02 | 1 | ||
| rs2492965 | 1.000 | 0.080 | 6 | 72445473 | intergenic variant | T/C | snv | 0.90 | 1 | ||
| rs2647006 | 1.000 | 0.080 | 6 | 32692805 | intergenic variant | A/C;G | snv | 1 | |||
| rs2647051 | 1.000 | 0.080 | 6 | 32703120 | downstream gene variant | T/C | snv | 0.64 | 1 | ||
| rs59888390 | 1.000 | 0.080 | 8 | 134989069 | regulatory region variant | A/G | snv | 0.25 | 1 | ||
| rs7332270 | 1.000 | 0.080 | 13 | 34857816 | intergenic variant | A/T | snv | 0.31 | 1 | ||
| rs75707332 | 1.000 | 0.080 | 12 | 22022003 | intergenic variant | G/A | snv | 1.6E-02 | 1 | ||
| rs76755915 | 1.000 | 0.080 | 4 | 97038456 | intergenic variant | G/C | snv | 1.7E-02 | 1 | ||
| rs76810409 | 1.000 | 0.080 | 7 | 109456395 | TF binding site variant | C/T | snv | 2.5E-02 | 1 | ||
| rs769398333 | 1.000 | 0.080 | 12 | 8857954 | missense variant | C/A;T | snv | 1.6E-05 | 1 | ||
| rs72799981 | 1.000 | 0.080 | 5 | 143150821 | intron variant | T/C | snv | 1.5E-02 | 1 | ||
| rs1484994 | 1.000 | 0.080 | 20 | 31718172 | intron variant | A/G | snv | 0.38 | 1 | ||
| rs9104 | 1.000 | 0.080 | 6 | 26377921 | 3 prime UTR variant | G/A | snv | 0.16 | 1 | ||
| rs1063340 | 1.000 | 0.080 | 17 | 36088417 | 3 prime UTR variant | G/C;T | snv | 1 | |||
| rs3817655 | 1.000 | 0.080 | 17 | 35872637 | intron variant | A/T | snv | 0.27 | 1 | ||
| rs3733096 | 1.000 | 0.080 | 3 | 46202483 | 3 prime UTR variant | C/G | snv | 1.4E-03 | 1 | ||
| rs743660 | 1.000 | 0.080 | 3 | 46360527 | 3 prime UTR variant | G/A | snv | 0.20 | 1 | ||
| rs708564 | 1.000 | 0.080 | 11 | 2388869 | intron variant | C/T | snv | 0.62 | 1 | ||
| rs28372683 | 1.000 | 0.080 | 19 | 45038140 | 3 prime UTR variant | G/A;T | snv | 1 | |||
| rs3128925 | 1.000 | 0.080 | 6 | 33103823 | non coding transcript exon variant | C/A;T | snv | 1 | |||
| rs1052020291 | 1.000 | 0.080 | 8 | 11848075 | missense variant | G/C | snv | 7.0E-06 | 1 | ||
| rs200664537 | 1.000 | 0.080 | 8 | 11847084 | missense variant | G/A;C | snv | 4.0E-06; 1.2E-04 | 1 | ||
| rs775321729 | 1.000 | 0.080 | 8 | 11845687 | missense variant | G/A;C | snv | 2.0E-05; 4.0E-06 | 1 |