| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs66561647 | 8 | 127959615 | intron variant | C/A;T | snv | 1 | |||||
| rs6992123 | 8 | 127978488 | intron variant | A/G | snv | 0.18 | 1 | ||||
| rs4733789 | 8 | 127822157 | intron variant | C/G;T | snv | 1 | |||||
| rs6992491 | 8 | 128185657 | intron variant | C/G | snv | 0.25 | 1 | ||||
| rs12676304 | 8 | 128151049 | intron variant | A/C | snv | 0.24 | 1 | ||||
| rs6470589 | 1.000 | 0.120 | 8 | 127877126 | intron variant | C/A;G | snv | 1 | |||
| rs6470588 | 1.000 | 0.120 | 8 | 127877125 | intron variant | A/C | snv | 0.53 | 1 | ||
| rs35252396 | 1.000 | 0.120 | 8 | 127877125 | intron variant | AC/CG | mnv | 1 | |||
| rs1499364 | 8 | 128167680 | intron variant | A/G | snv | 0.26 | 1 | ||||
| rs12548864 | 8 | 127916000 | intron variant | C/T | snv | 0.27 | 1 | ||||
| rs2608053 | 1.000 | 0.120 | 8 | 128063586 | intron variant | T/C | snv | 0.50 | 1 | ||
| rs4733823 | 8 | 128002451 | intron variant | C/A;T | snv | 0.47 | 1 | ||||
| rs13280095 | 1.000 | 0.080 | 8 | 128166844 | intron variant | A/C | snv | 0.26 | 1 | ||
| rs12156002 | 1.000 | 0.080 | 8 | 128178298 | intron variant | C/A | snv | 0.24 | 1 | ||
| rs759648 | 1.000 | 0.080 | 8 | 128146699 | intron variant | A/C | snv | 0.33 | 1 | ||
| rs4410871 | 0.925 | 0.080 | 8 | 127802783 | intron variant | T/C | snv | 0.74 | 1 | ||
| rs13255292 | 0.925 | 0.120 | 8 | 128064327 | intron variant | C/T | snv | 0.24 | 1 | ||
| rs10956401 | 8 | 127990173 | non coding transcript exon variant | G/A | snv | 0.31 | 1 | ||||
| rs11780156 | 0.925 | 0.080 | 8 | 128182395 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs9886651 | 1.000 | 0.120 | 8 | 127805637 | intron variant | A/G | snv | 0.35 | 1 | ||
| rs66824612 | 8 | 127955573 | intron variant | C/T | snv | 0.29 | 1 | ||||
| rs6990534 | 8 | 127801845 | intron variant | A/G | snv | 0.68 | 1 | ||||
| rs6470578 | 1.000 | 0.120 | 8 | 127797311 | intron variant | T/A | snv | 0.73 | 1 | ||
| rs10956412 | 1.000 | 0.040 | 8 | 128150251 | intron variant | A/C;G | snv | 1 | |||
| rs2608029 | 1.000 | 0.040 | 8 | 128157880 | intron variant | C/G | snv | 0.37 | 2 |