| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs118101777 | 0.614 | 0.280 | 15 | 90087472 | missense variant | C/T | snv | 2.0E-03 | 1.6E-03 | 42 | |
| rs11540478 | 0.851 | 0.080 | 15 | 90085305 | synonymous variant | G/A;C | snv | 3.5E-02; 6.4E-06 | 4 | ||
| rs1805794 | 0.605 | 0.600 | 8 | 89978251 | missense variant | C/G | snv | 0.35 | 0.31 | 41 | |
| rs709816 | 0.752 | 0.320 | 8 | 89955483 | synonymous variant | A/G | snv | 0.47 | 0.51 | 10 | |
| rs2735383 | 0.708 | 0.360 | 8 | 89935041 | 3 prime UTR variant | C/G | snv | 0.31 | 18 | ||
| rs1063054 | 0.807 | 0.160 | 8 | 89934373 | 3 prime UTR variant | T/G | snv | 0.32 | 6 | ||
| rs13312986 | 0.882 | 0.080 | 8 | 89933890 | 3 prime UTR variant | T/C | snv | 3.0E-02 | 3 | ||
| rs14448 | 0.882 | 0.080 | 8 | 89933605 | 3 prime UTR variant | A/G | snv | 0.19 | 3 | ||
| rs1663689 | 0.882 | 0.080 | 10 | 8983232 | intergenic variant | T/C | snv | 0.25 | 3 | ||
| rs372594677 | 1.000 | 0.080 | 3 | 89472571 | missense variant | C/A;T | snv | 8.0E-06; 1.2E-05 | 1 | ||
| rs4619206 | 1.000 | 0.080 | 12 | 893691 | intron variant | T/C | snv | 0.74 | 1 | ||
| rs2279574 | 0.827 | 0.120 | 12 | 89351700 | missense variant | C/A;T | snv | 0.52 | 8 | ||
| rs1926203 | 0.882 | 0.160 | 10 | 88967577 | intron variant | C/A | snv | 0.59 | 3 | ||
| rs7953330 | 0.925 | 0.080 | 12 | 889653 | intron variant | G/C | snv | 0.28 | 2 | ||
| rs2869967 | 0.827 | 0.120 | 4 | 88948181 | intron variant | T/C | snv | 0.49 | 11 | ||
| rs4673 | 0.653 | 0.600 | 16 | 88646828 | missense variant | A/G;T | snv | 0.70 | 32 | ||
| rs2231142 | 0.583 | 0.680 | 4 | 88131171 | missense variant | G/C;T | snv | 4.0E-06; 0.12 | 56 | ||
| rs1205454520 | 0.763 | 0.120 | 10 | 87864059 | 5 prime UTR variant | -/G | delins | 7.2E-06 | 10 | ||
| rs2188524 | 0.882 | 0.080 | 7 | 87601119 | intron variant | T/C | snv | 3.2E-03 | 3 | ||
| rs149518139 | 0.882 | 0.080 | 7 | 87566852 | missense variant | T/C | snv | 4.0E-06 | 3 | ||
| rs1128503 | 0.564 | 0.760 | 7 | 87550285 | synonymous variant | A/G | snv | 0.54 | 0.63 | 64 | |
| rs2235013 | 0.882 | 0.080 | 7 | 87549310 | intron variant | C/T | snv | 0.46 | 0.48 | 3 | |
| rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
| rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
| rs3842 | 0.882 | 0.080 | 7 | 87504050 | 3 prime UTR variant | T/C | snv | 0.16 | 5 |