| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10106652 | 1.000 | 0.040 | 8 | 20070649 | intergenic variant | G/A | snv | 0.29 | 3 | ||
| rs12423664 | 1.000 | 0.040 | 12 | 132493308 | intron variant | G/A | snv | 0.10 | 6 | ||
| rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 16 | ||
| rs12801636 | 1.000 | 0.040 | 11 | 65623846 | intron variant | G/A | snv | 0.25 | 5 | ||
| rs15285 | 1.000 | 0.040 | 8 | 19967156 | 3 prime UTR variant | C/T | snv | 0.36 | 5 | ||
| rs1800978 | 1.000 | 0.040 | 9 | 104903697 | 5 prime UTR variant | C/A;G;T | snv | 5.4E-06; 0.14 | 6 | ||
| rs1801706 | 1.000 | 0.040 | 16 | 56983750 | 3 prime UTR variant | G/A | snv | 0.17 | 3 | ||
| rs2001844 | 0.882 | 0.040 | 8 | 125466503 | upstream gene variant | A/G | snv | 0.43 | 9 | ||
| rs2074158 | 1.000 | 0.040 | 17 | 42105145 | missense variant | T/C | snv | 0.21 | 0.33 | 2 | |
| rs2144300 | 0.882 | 0.040 | 1 | 230159169 | intron variant | C/T | snv | 0.44 | 7 | ||
| rs2257129 | 1.000 | 0.040 | 10 | 121139183 | regulatory region variant | T/C | snv | 0.82 | 3 | ||
| rs2281719 | 1.000 | 0.040 | 1 | 230161913 | intron variant | C/T | snv | 0.45 | 4 | ||
| rs2472386 | 1.000 | 0.040 | 9 | 104839260 | intron variant | G/A | snv | 0.47 | 3 | ||
| rs247616 | 1.000 | 0.040 | 16 | 56955678 | intergenic variant | C/T | snv | 0.29 | 8 | ||
| rs255052 | 0.925 | 0.040 | 16 | 67991092 | intron variant | G/A | snv | 0.17 | 0.17 | 4 | |
| rs2814944 | 1.000 | 0.040 | 6 | 34585020 | downstream gene variant | G/A | snv | 0.20 | 3 | ||
| rs2880301 | 1.000 | 0.040 | 13 | 19526394 | intron variant | C/T | snv | 4 | |||
| rs2967605 | 0.925 | 0.040 | 19 | 8404854 | downstream gene variant | C/T | snv | 0.20 | 4 | ||
| rs2972146 | 0.882 | 0.040 | 2 | 226235982 | intergenic variant | G/T | snv | 0.72 | 9 | ||
| rs35237252 | 1.000 | 0.040 | 8 | 20012760 | intergenic variant | C/A;T | snv | 0.24 | 2 | ||
| rs5167 | 1.000 | 0.040 | 19 | 44945208 | missense variant | T/A;G | snv | 3.6E-05; 0.39 | 7 | ||
| rs5880 | 0.827 | 0.040 | 16 | 56981179 | missense variant | G/C | snv | 5.2E-02 | 3.7E-02 | 10 | |
| rs5883 | 1.000 | 0.040 | 16 | 56973441 | synonymous variant | C/T | snv | 5.1E-02 | 6.6E-02 | 5 | |
| rs895953 | 1.000 | 0.040 | 12 | 121811142 | intron variant | G/T | snv | 0.76 | 5 | ||
| rs9326246 | 0.925 | 0.040 | 11 | 116741017 | intergenic variant | C/G | snv | 0.93 | 9 |