| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3219476 | 0.882 | 0.200 | 1 | 45336998 | intron variant | A/C | snv | 0.58 | 3 | ||
| rs437179 | 0.882 | 0.160 | 6 | 31961237 | missense variant | A/C | snv | 0.76 | 0.78 | 3 | |
| rs1042127 | 0.925 | 0.120 | 6 | 31116393 | missense variant | A/C | snv | 0.21 | 0.17 | 2 | |
| rs2076538 | 1.000 | 0.120 | 6 | 32349694 | non coding transcript exon variant | A/C | snv | 0.42 | 0.33 | 2 | |
| rs2524095 | 0.925 | 0.160 | 6 | 31298340 | intron variant | A/C | snv | 0.65 | 2 | ||
| rs2858884 | 0.925 | 0.200 | 6 | 32732306 | upstream gene variant | A/C | snv | 0.23 | 2 | ||
| rs3781094 | 1.000 | 0.120 | 10 | 8059464 | intron variant | A/C | snv | 0.52 | 2 | ||
| rs518374 | 1.000 | 0.120 | 6 | 32297933 | intron variant | A/C | snv | 0.33 | 2 | ||
| rs9268862 | 0.925 | 0.160 | 6 | 32462390 | intron variant | A/C | snv | 0.29 | 2 | ||
| rs11121380 | 1.000 | 0.120 | 1 | 9348900 | intron variant | A/C | snv | 0.11 | 1 | ||
| rs11765576 | 1.000 | 0.120 | 7 | 131676169 | intergenic variant | A/C | snv | 0.47 | 1 | ||
| rs12110787 | 1.000 | 0.120 | 6 | 161053934 | intron variant | A/C | snv | 0.16 | 1 | ||
| rs1480383 | 1.000 | 0.120 | 6 | 32773079 | intergenic variant | A/C | snv | 0.31 | 1 | ||
| rs1689334 | 1.000 | 0.120 | 7 | 52992421 | intergenic variant | A/C | snv | 1 | |||
| rs16906916 | 1.000 | 0.120 | 10 | 55089225 | intron variant | A/C | snv | 3.9E-02 | 1 | ||
| rs17638585 | 1.000 | 0.120 | 16 | 27097815 | regulatory region variant | A/C | snv | 0.15 | 1 | ||
| rs2395161 | 1.000 | 0.120 | 6 | 32419975 | intergenic variant | A/C | snv | 0.13 | 1 | ||
| rs2532919 | 1.000 | 0.120 | 6 | 30966198 | upstream gene variant | A/C | snv | 0.18 | 1 | ||
| rs2844605 | 1.000 | 0.120 | 6 | 31280814 | non coding transcript exon variant | A/C | snv | 0.46 | 1 | ||
| rs3096700 | 1.000 | 0.120 | 6 | 32254005 | upstream gene variant | A/C | snv | 0.63 | 1 | ||
| rs3129869 | 1.000 | 0.120 | 6 | 32437894 | upstream gene variant | A/C | snv | 0.62 | 1 | ||
| rs3129927 | 1.000 | 0.120 | 6 | 32366050 | intron variant | A/C | snv | 7.3E-02 | 9.3E-02 | 1 | |
| rs3132680 | 1.000 | 0.120 | 6 | 30105418 | non coding transcript exon variant | A/C | snv | 0.73 | 1 | ||
| rs3135380 | 1.000 | 0.120 | 6 | 32416900 | intergenic variant | A/C | snv | 0.13 | 1 | ||
| rs35690726 | 1.000 | 0.120 | 5 | 115513027 | non coding transcript exon variant | A/C | snv | 1.5E-02 | 1 |