| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11542041 | 0.677 | 0.480 | 19 | 44908690 | missense variant | C/A;T | snv | 2.1E-05 | 23 | ||
| rs11556924 | 0.752 | 0.240 | 7 | 130023656 | missense variant | C/A;T | snv | 4.0E-06; 0.28 | 21 | ||
| rs11571836 | 0.827 | 0.200 | 13 | 32399302 | 3 prime UTR variant | A/G;T | snv | 6 | |||
| rs11572325 | 0.925 | 0.080 | 1 | 59896030 | intron variant | A/T | snv | 0.12 | 3 | ||
| rs11574914 | 0.925 | 0.200 | 9 | 34710341 | intron variant | G/A | snv | 0.24 | 2 | ||
| rs11574915 | 1.000 | 0.080 | 9 | 34710087 | 5 prime UTR variant | A/C;G | snv | 0.13; 4.1E-06 | 1 | ||
| rs11575937 | 0.653 | 0.480 | 1 | 156136985 | missense variant | G/A;T | snv | 29 | |||
| rs11591147 | 0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 | 28 | ||
| rs11614913 | 0.512 | 0.760 | 12 | 53991815 | mature miRNA variant | C/T | snv | 0.39 | 0.34 | 111 | |
| rs11666735 | 1.000 | 0.080 | 19 | 54885501 | missense variant | G/A | snv | 6.9E-02 | 6.6E-02 | 1 | |
| rs1169286 | 1.000 | 0.080 | 12 | 120981253 | intron variant | T/C | snv | 0.39 | 3 | ||
| rs11739136 | 0.827 | 0.200 | 5 | 170383792 | missense variant | C/T | snv | 9.9E-02 | 8.7E-02 | 10 | |
| rs11748327 | 1.000 | 0.080 | 5 | 4029676 | downstream gene variant | C/T | snv | 0.21 | 2 | ||
| rs117714106 | 0.882 | 0.080 | 14 | 84338144 | intergenic variant | C/T | snv | 9.1E-03 | 3 | ||
| rs1177506410 | 0.776 | 0.240 | 1 | 230706148 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 12 | |
| rs11786580 | 0.925 | 0.160 | 8 | 58493381 | intron variant | C/T | snv | 0.19 | 2 | ||
| rs1183194405 | 0.716 | 0.440 | 11 | 46719773 | missense variant | G/A;T | snv | 4.5E-06; 4.5E-06 | 19 | ||
| rs1188254133 | 0.851 | 0.240 | 6 | 43781990 | missense variant | T/G | snv | 7.0E-06 | 4 | ||
| rs1188383936 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 102 | ||
| rs12026 | 0.827 | 0.240 | 7 | 95411704 | missense variant | G/C | snv | 0.27 | 0.27 | 6 | |
| rs12027041 | 1.000 | 0.080 | 1 | 3674884 | intron variant | G/C | snv | 0.38 | 1 | ||
| rs12041331 | 0.776 | 0.200 | 1 | 156899922 | intron variant | G/A | snv | 0.19 | 11 | ||
| rs12118721 | 1.000 | 0.080 | 1 | 154424940 | intron variant | T/C | snv | 0.51 | 1 | ||
| rs1213545562 | 1.000 | 0.080 | 11 | 2166984 | synonymous variant | G/A | snv | 9.6E-06 | 2 | ||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 |