| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10945859 | 0.882 | 0.120 | 6 | 162721570 | intron variant | T/C | snv | 0.17 | 3 | ||
| rs111200466 | 1.000 | 0.080 | 4 | 153684312 | 5 prime UTR variant | CGGCTGCTCGGCGTTCTCTCAGG/- | delins | 0.17 | 2 | ||
| rs111511318 | 1.000 | 0.080 | 5 | 156998817 | intergenic variant | C/A | snv | 2.9E-02 | 1 | ||
| rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 46 | |
| rs11249006 | 1.000 | 0.080 | 1 | 24155984 | 3 prime UTR variant | G/A | snv | 0.30 | 1 | ||
| rs1126579 | 0.776 | 0.200 | 2 | 218136011 | 3 prime UTR variant | T/C | snv | 0.62 | 8 | ||
| rs1127354 | 0.667 | 0.400 | 20 | 3213196 | missense variant | C/A;G | snv | 7.5E-02 | 26 | ||
| rs1128503 | 0.564 | 0.760 | 7 | 87550285 | synonymous variant | A/G | snv | 0.54 | 0.63 | 64 | |
| rs1130409 | 0.555 | 0.720 | 14 | 20456995 | missense variant | T/A;C;G | snv | 4.0E-06; 4.0E-06; 0.42 | 72 | ||
| rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 | |||
| rs1133763 | 0.882 | 0.200 | 17 | 34320812 | missense variant | A/C | snv | 0.21 | 0.15 | 4 | |
| rs1143629 | 0.882 | 0.160 | 2 | 112835941 | intron variant | G/A | snv | 0.60 | 3 | ||
| rs1143634 | 0.597 | 0.680 | 2 | 112832813 | synonymous variant | G/A | snv | 0.19 | 0.19 | 52 | |
| rs11506105 | 0.851 | 0.160 | 7 | 55152484 | intron variant | A/G | snv | 0.59 | 4 | ||
| rs1156458285 | 1.000 | 0.080 | 9 | 21440717 | missense variant | G/C | snv | 1 | |||
| rs11574129 | 0.882 | 0.160 | 12 | 47843520 | 3 prime UTR variant | A/G | snv | 1.6E-02 | 3 | ||
| rs116399066 | 1.000 | 0.080 | 1 | 143723149 | upstream gene variant | C/A;T | snv | 1 | |||
| rs117648444 | 0.882 | 0.160 | 19 | 39247938 | missense variant | G/A | snv | 0.25 | 8.1E-02 | 3 | |
| rs1178326401 | 1.000 | 0.080 | 11 | 46728826 | synonymous variant | G/A | snv | 4.0E-06 | 1 | ||
| rs11790131 | 0.882 | 0.080 | 9 | 19469848 | intergenic variant | G/A;T | snv | 6 | |||
| rs11820062 | 0.925 | 0.120 | 11 | 65662465 | 5 prime UTR variant | T/C | snv | 0.52 | 3 | ||
| rs11881222 | 0.925 | 0.080 | 19 | 39244283 | intron variant | A/G | snv | 0.30 | 3 | ||
| rs1207011218 | 0.742 | 0.440 | 2 | 203870794 | synonymous variant | C/T | snv | 12 | |||
| rs12075 | 0.724 | 0.240 | 1 | 159205564 | missense variant | G/A | snv | 0.51 | 0.66 | 22 | |
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 |