| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10761659 | 0.925 | 0.040 | 10 | 62685804 | intron variant | A/G | snv | 0.43 | 2 | ||
| rs10781499 | 0.925 | 0.040 | 9 | 136371953 | synonymous variant | G/A | snv | 0.41 | 0.38 | 2 | |
| rs10789230 | 1.000 | 0.040 | 1 | 67264945 | downstream gene variant | G/C;T | snv | 1 | |||
| rs10801047 | 1.000 | 0.040 | 1 | 191590226 | intergenic variant | A/T | snv | 0.82 | 1 | ||
| rs10865331 | 0.827 | 0.120 | 2 | 62324337 | intergenic variant | A/G | snv | 0.57 | 3 | ||
| rs10883365 | 0.882 | 0.080 | 10 | 99528007 | non coding transcript exon variant | G/A | snv | 0.52 | 1 | ||
| rs10886462 | 1.000 | 0.040 | 10 | 119345799 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs10889676 | 0.827 | 0.120 | 1 | 67256884 | intron variant | C/A;T | snv | 1 | |||
| rs10889677 | 0.627 | 0.720 | 1 | 67259437 | 3 prime UTR variant | C/A | snv | 0.27 | 2 | ||
| rs10947261 | 0.882 | 0.240 | 6 | 32405455 | splice region variant | G/T | snv | 0.11 | 4 | ||
| rs10975003 | 0.882 | 0.080 | 9 | 5213687 | intergenic variant | T/C | snv | 0.43 | 1 | ||
| rs10995271 | 0.776 | 0.280 | 10 | 62678726 | downstream gene variant | G/C | snv | 0.32 | 3 | ||
| rs11010067 | 0.925 | 0.040 | 10 | 35006503 | downstream gene variant | C/G | snv | 0.37 | 1 | ||
| rs1105267 | 1.000 | 0.040 | 13 | 20365097 | intergenic variant | G/A | snv | 0.54 | 1 | ||
| rs1109863 | 1.000 | 0.040 | 16 | 50658453 | intergenic variant | G/A | snv | 0.69 | 1 | ||
| rs11167764 | 0.925 | 0.120 | 5 | 142099500 | regulatory region variant | A/C | snv | 0.80 | 2 | ||
| rs11168249 | 0.807 | 0.120 | 12 | 47814585 | intron variant | T/C | snv | 0.50 | 2 | ||
| rs11175593 | 0.882 | 0.160 | 12 | 40208138 | non coding transcript exon variant | C/T | snv | 2.8E-02 | 3 | ||
| rs11190140 | 0.827 | 0.160 | 10 | 99531836 | upstream gene variant | T/C | snv | 0.55 | 4 | ||
| rs11190141 | 1.000 | 0.040 | 10 | 99532633 | upstream gene variant | C/T | snv | 0.40 | 1 | ||
| rs11195128 | 1.000 | 0.040 | 10 | 110426390 | downstream gene variant | C/G;T | snv | 1 | |||
| rs11208994 | 1.000 | 0.040 | 1 | 67059360 | regulatory region variant | A/G;T | snv | 1 | |||
| rs11209002 | 1.000 | 0.040 | 1 | 67124778 | intron variant | T/C | snv | 0.77 | 1 | ||
| rs11209003 | 1.000 | 0.040 | 1 | 67135449 | intron variant | G/T | snv | 0.28 | 1 | ||
| rs11209008 | 0.882 | 0.080 | 1 | 67157615 | intron variant | G/A;T | snv | 5.7E-02 | 1 |