| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12110693 | 6 | 121837124 | intergenic variant | G/A | snv | 0.23 | 1 | ||||
| rs12440667 | 1.000 | 0.040 | 15 | 73939098 | intron variant | C/A;T | snv | 1 | |||
| rs12454712 | 0.925 | 0.120 | 18 | 63178651 | intron variant | T/A;C | snv | 1 | |||
| rs12731740 | 1 | 207851475 | intron variant | C/T | snv | 9.1E-02 | 1 | ||||
| rs1294410 | 6 | 6738519 | intron variant | T/C | snv | 0.65 | 1 | ||||
| rs1294421 | 1.000 | 0.040 | 6 | 6742916 | upstream gene variant | T/A;C;G | snv | 1 | |||
| rs1406948 | 20 | 35317816 | intron variant | G/A | snv | 0.44 | 1 | ||||
| rs143384 | 0.827 | 0.200 | 20 | 35437976 | 5 prime UTR variant | G/A | snv | 0.44 | 1 | ||
| rs1443512 | 12 | 53948900 | downstream gene variant | A/C;T | snv | 1 | |||||
| rs15285 | 1.000 | 0.040 | 8 | 19967156 | 3 prime UTR variant | C/T | snv | 0.36 | 1 | ||
| rs17109256 | 14 | 79473650 | intron variant | G/A | snv | 0.21 | 1 | ||||
| rs17213965 | 16 | 15788110 | intron variant | C/T | snv | 0.24 | 1 | ||||
| rs17568628 | 5 | 76751114 | intergenic variant | T/C;G | snv | 1 | |||||
| rs1993709 | 1.000 | 0.080 | 1 | 72372846 | intron variant | A/G | snv | 0.85 | 1 | ||
| rs2119690 | 8 | 20002028 | intergenic variant | G/A;C | snv | 1 | |||||
| rs2145272 | 20 | 6645571 | intergenic variant | G/A;T | snv | 1 | |||||
| rs2235529 | 1.000 | 0.040 | 1 | 22123994 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs2820464 | 1 | 219519878 | intergenic variant | G/A;C | snv | 1 | |||||
| rs2894204 | 1.000 | 0.040 | 6 | 31269284 | intron variant | C/A;T | snv | 1 | |||
| rs3088050 | 5 | 177299634 | 3 prime UTR variant | G/A | snv | 0.18 | 1 | ||||
| rs3786897 | 1.000 | 0.080 | 19 | 33402102 | intron variant | A/G | snv | 0.45 | 1 | ||
| rs4580892 | 6 | 127088737 | intron variant | C/T | snv | 0.32 | 1 | ||||
| rs459193 | 0.925 | 0.120 | 5 | 56510924 | downstream gene variant | A/G | snv | 0.69 | 1 | ||
| rs4640244 | 17 | 21380911 | intron variant | A/G | snv | 0.33 | 1 | ||||
| rs4686340 | 3 | 9303534 | intron variant | A/C | snv | 0.80 | 1 |