| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17531933 | 11 | 56128173 | downstream gene variant | T/C;G | snv | 1 | |||||
| rs17598045 | 11 | 55940815 | upstream gene variant | G/A;T | snv | 1 | |||||
| rs1867226 | 15 | 90980483 | non coding transcript exon variant | C/A;G | snv | 1 | |||||
| rs2004776 | 1 | 230712956 | intron variant | C/G;T | snv | 1 | |||||
| rs2702888 | 8 | 6907510 | intergenic variant | G/A;C;T | snv | 1 | |||||
| rs2969070 | 7 | 2472910 | downstream gene variant | G/A;C | snv | 1 | |||||
| rs301819 | 0.882 | 0.120 | 1 | 8441726 | intron variant | A/G;T | snv | 1 | |||
| rs3751664 | 16 | 1204369 | missense variant | C/A;T | snv | 9.4E-06; 8.2E-02 | 1 | ||||
| rs3789671 | 1 | 230708054 | intron variant | G/A;T | snv | 1 | |||||
| rs4685307 | 3 | 16123911 | regulatory region variant | G/A;T | snv | 1 | |||||
| rs4846049 | 0.776 | 0.360 | 1 | 11790308 | 3 prime UTR variant | T/A;G | snv | 1 | |||
| rs4977950 | 9 | 24732484 | intergenic variant | G/C;T | snv | 1 | |||||
| rs5051 | 0.882 | 0.160 | 1 | 230714126 | intron variant | C/A;G;T | snv | 1 | |||
| rs6567041 | 18 | 58975551 | intron variant | A/G;T | snv | 1 | |||||
| rs6763470 | 3 | 55390915 | intergenic variant | T/A;G | snv | 1 | |||||
| rs6782531 | 3 | 61009928 | intron variant | G/C;T | snv | 1 | |||||
| rs7591163 | 2 | 227850659 | intergenic variant | C/A;G;T | snv | 1 | |||||
| rs7726475 | 5 | 32575808 | intron variant | G/A;C | snv | 1 | |||||
| rs7936086 | 11 | 55923383 | intergenic variant | C/A;T | snv | 1 | |||||
| rs7984522 | 13 | 108695311 | intron variant | T/A;C | snv | 1 | |||||
| rs825937 | 2 | 4760437 | intergenic variant | C/A;T | snv | 1 | |||||
| rs871606 | 4 | 53933078 | intron variant | T/C;G | snv | 1 | |||||
| rs9663362 | 10 | 94135420 | intron variant | G/A;C | snv | 1 | |||||
| rs72912698 | 6 | 84882143 | intergenic variant | C/T | snv | 7.7E-04 | 1 | ||||
| rs576853093 | 1 | 11790946 | intron variant | -/C;CACACACACACAC | ins | 6.2E-03 | 1 |