| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7976059 | 0.882 | 0.160 | 12 | 51857488 | downstream gene variant | G/T | snv | 0.35 | 4 | ||
| rs13302855 | 0.882 | 0.200 | 9 | 27595997 | intergenic variant | C/T | snv | 7.5E-02 | 3 | ||
| rs11224052 | 1.000 | 0.080 | 11 | 134870879 | intergenic variant | G/A;T | snv | 0.27 | 1 | ||
| rs1361121 | 1.000 | 0.080 | 6 | 49956357 | downstream gene variant | A/C | snv | 6.3E-02 | 1 | ||
| rs1517166 | 1.000 | 0.080 | 18 | 64030063 | intergenic variant | T/C | snv | 0.50 | 1 | ||
| rs1971791 | 1.000 | 0.080 | 15 | 70283799 | intergenic variant | G/A | snv | 0.45 | 1 | ||
| rs1982915 | 1.000 | 0.080 | 9 | 27579562 | intergenic variant | A/G | snv | 0.48 | 1 | ||
| rs2453556 | 1.000 | 0.080 | 9 | 27586164 | intergenic variant | A/G | snv | 0.46 | 1 | ||
| rs2477518 | 1.000 | 0.080 | 9 | 27599748 | intergenic variant | T/C | snv | 0.47 | 1 | ||
| rs2785946 | 1.000 | 0.080 | 13 | 54355063 | regulatory region variant | A/G | snv | 0.72 | 1 | ||
| rs2838568 | 1.000 | 0.080 | 21 | 44476857 | upstream gene variant | G/A | snv | 0.40 | 1 | ||
| rs284793 | 1.000 | 0.080 | 4 | 99409137 | downstream gene variant | G/A | snv | 0.26 | 1 | ||
| rs3113494 | 1.000 | 0.080 | 4 | 86911448 | intron variant | G/A | snv | 0.40 | 1 | ||
| rs4363506 | 1.000 | 0.080 | 10 | 127476239 | intergenic variant | T/C | snv | 0.41 | 1 | ||
| rs5937496 | 1.000 | 0.080 | X | 76127599 | regulatory region variant | G/A | snv | 0.16 | 1 | ||
| rs6080539 | 1.000 | 0.080 | 20 | 17048849 | intergenic variant | T/C | snv | 0.32 | 1 | ||
| rs6985069 | 1.000 | 0.080 | 8 | 28228571 | downstream gene variant | G/A | snv | 0.67 | 1 | ||
| rs7000234 | 1.000 | 0.080 | 8 | 80624879 | downstream gene variant | G/A | snv | 0.10 | 1 | ||
| rs7577894 | 1.000 | 0.080 | 2 | 55781769 | regulatory region variant | T/C;G | snv | 1 | |||
| rs855913 | 1.000 | 0.080 | 7 | 149506571 | intergenic variant | A/C | snv | 0.96 | 1 | ||
| rs945699 | 1.000 | 0.080 | 1 | 227905618 | regulatory region variant | A/G | snv | 0.41 | 1 | ||
| rs9901522 | 1.000 | 0.080 | 17 | 14770617 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs780912099 | 1.000 | 0.080 | 20 | 31721806 | missense variant | C/G | snv | 4.0E-06 | 1 | ||
| rs772365758 | 1.000 | 0.080 | 3 | 186854228 | missense variant | G/A | snv | 8.0E-06 | 2.1E-05 | 1 | |
| rs756309139 | 1.000 | 0.080 | 6 | 31616139 | missense variant | G/A;C | snv | 8.3E-06; 2.1E-05 | 1 |