| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11202592 | 0.851 | 0.200 | 10 | 87864461 | 5 prime UTR variant | C/G | snv | 3.8E-03 | 1.4E-03 | 5 | |
| rs11228565 | 0.882 | 0.160 | 11 | 69211113 | regulatory region variant | G/A | snv | 0.16 | 3 | ||
| rs11237828 | 1.000 | 0.120 | 11 | 79422176 | mature miRNA variant | T/C | snv | 0.12 | 0.22 | 1 | |
| rs11249433 | 0.827 | 0.160 | 1 | 121538815 | intron variant | A/C;G | snv | 9 | |||
| rs1130233 | 0.742 | 0.480 | 14 | 104773557 | synonymous variant | C/T | snv | 0.30 | 0.23 | 13 | |
| rs1131691003 | 0.752 | 0.360 | 17 | 7676381 | splice donor variant | C/A;G | snv | 12 | |||
| rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 | |||
| rs1131691042 | 0.752 | 0.360 | 17 | 7675052 | splice donor variant | C/T | snv | 12 | |||
| rs115214213 | 1.000 | 0.120 | 11 | 35231896 | 3 prime UTR variant | T/C | snv | 4.9E-03 | 1 | ||
| rs11540652 | 0.592 | 0.640 | 17 | 7674220 | missense variant | C/A;G;T | snv | 1.2E-05 | 57 | ||
| rs1154865 | 0.882 | 0.160 | 12 | 73596057 | intergenic variant | C/G | snv | 0.22 | 3 | ||
| rs11556218 | 0.653 | 0.600 | 15 | 81305928 | missense variant | T/G | snv | 9.6E-02 | 0.12 | 27 | |
| rs11614913 | 0.512 | 0.760 | 12 | 53991815 | mature miRNA variant | C/T | snv | 0.39 | 0.34 | 111 | |
| rs11668878 | 0.925 | 0.200 | 19 | 46765116 | intron variant | G/T | snv | 5.1E-02 | 2 | ||
| rs11730582 | 0.807 | 0.240 | 4 | 87975269 | non coding transcript exon variant | T/C | snv | 0.37 | 10 | ||
| rs117465650 | 1.000 | 0.120 | 2 | 55050090 | missense variant | C/T | snv | 0.12 | 6.1E-02 | 1 | |
| rs117565607 | 1.000 | 0.120 | 6 | 30204594 | intron variant | T/A | snv | 2.3E-03 | 1 | ||
| rs11865086 | 1.000 | 0.120 | 16 | 30119172 | intron variant | C/A | snv | 0.55 | 1 | ||
| rs11978267 | 0.763 | 0.240 | 7 | 50398606 | intron variant | A/G | snv | 0.25 | 9 | ||
| rs121912651 | 0.605 | 0.680 | 17 | 7674221 | missense variant | G/A;C | snv | 4.0E-06 | 53 | ||
| rs121913483 | 0.649 | 0.560 | 4 | 1801841 | missense variant | C/A;G;T | snv | 4.2E-06; 1.3E-05 | 31 | ||
| rs1219648 | 0.716 | 0.320 | 10 | 121586676 | intron variant | A/G;T | snv | 17 | |||
| rs12220909 | 0.827 | 0.240 | 10 | 14383222 | mature miRNA variant | G/C;T | snv | 4.9E-03 | 5 | ||
| rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
| rs12500426 | 0.851 | 0.240 | 4 | 94593458 | intron variant | A/C | snv | 0.54 | 5 |