| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4081134 | 0.790 | 0.160 | 14 | 100855451 | non coding transcript exon variant | G/A | snv | 0.29 | 7 | ||
| rs745805222 | 0.790 | 0.120 | 12 | 102475722 | synonymous variant | C/T | snv | 1.2E-05 | 4.9E-05 | 7 | |
| rs10895322 | 0.851 | 0.120 | 11 | 102599525 | intron variant | A/G | snv | 9.4E-02 | 4 | ||
| rs2094258 | 0.701 | 0.280 | 13 | 102844409 | intron variant | C/T | snv | 0.18 | 20 | ||
| rs1047768 | 0.695 | 0.320 | 13 | 102852167 | synonymous variant | T/C | snv | 0.52 | 0.59 | 20 | |
| rs873601 | 0.677 | 0.360 | 13 | 102875987 | 3 prime UTR variant | G/A | snv | 0.59 | 25 | ||
| rs41274458 | 0.851 | 0.080 | 1 | 10303606 | missense variant | G/T | snv | 1.8E-02 | 1.9E-02 | 4 | |
| rs758576072 | 0.851 | 0.160 | 8 | 104244917 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 4 | ||
| rs2302616 | 0.882 | 0.080 | 2 | 10448065 | intron variant | C/A | snv | 0.26 | 3 | ||
| rs72990858 | 1.000 | 0.040 | 6 | 104699909 | intergenic variant | G/A | snv | 7.4E-02 | 1 | ||
| rs4336470 | 1.000 | 0.040 | 6 | 104732910 | intron variant | C/T | snv | 0.45 | 1 | ||
| rs9404576 | 0.882 | 0.160 | 6 | 104736765 | intron variant | T/A;G | snv | 3 | |||
| rs4079063 | 1.000 | 0.040 | 6 | 104818243 | intron variant | A/G;T | snv | 1 | |||
| rs2499663 | 1.000 | 0.040 | 6 | 104852695 | intron variant | C/T | snv | 0.43 | 1 | ||
| rs2499667 | 1.000 | 0.040 | 6 | 104871250 | intron variant | G/A | snv | 0.43 | 1 | ||
| rs143864187 | 0.882 | 0.080 | 11 | 104949666 | missense variant | C/A | snv | 3 | |||
| rs17065417 | 0.882 | 0.080 | 6 | 104958399 | intron variant | A/C | snv | 0.10 | 3 | ||
| rs221634 | 0.851 | 0.080 | 6 | 105080213 | 3 prime UTR variant | T/A | snv | 0.52 | 4 | ||
| rs4884357 | 0.807 | 0.120 | 1 | 11022301 | missense variant | G/A;T | snv | 4.0E-06 | 6 | ||
| rs367543041 | 0.742 | 0.200 | 1 | 11022553 | missense variant | G/A;C | snv | 3.0E-05 | 15 | ||
| rs4938723 | 0.574 | 0.680 | 11 | 111511840 | intron variant | T/C | snv | 0.32 | 60 | ||
| rs148634289 | 0.827 | 0.200 | 11 | 112088925 | synonymous variant | C/T | snv | 1.6E-05 | 2.1E-05 | 6 | |
| rs397507509 | 0.807 | 0.240 | 12 | 112450359 | missense variant | G/C;T | snv | 9 | |||
| rs2153977 | 0.807 | 0.240 | 1 | 113537449 | intron variant | C/T | snv | 0.28 | 6 | ||
| rs2273267 | 0.882 | 0.080 | 1 | 114716848 | upstream gene variant | A/C;T | snv | 4 |