Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2073617 | 0.776 | 0.360 | 8 | 118952044 | upstream gene variant | G/A | snv | 0.58 | 1 | ||
| rs2073618 | 0.716 | 0.480 | 8 | 118951813 | missense variant | G/C | snv | 0.52 | 0.60 | 1 | |
| rs11573829 | 8 | 118947384 | intron variant | T/A;C | snv | 1 | |||||
| rs11573885 | 8 | 118936926 | intron variant | T/C | snv | 0.45 | 1 | ||||
| rs1485289 | 8 | 118942040 | intron variant | G/A | snv | 0.60 | 1 | ||||
| rs1905786 | 1.000 | 0.040 | 8 | 118939453 | intron variant | T/A;C | snv | 1 | |||
| rs3134063 | 8 | 118947418 | intron variant | C/G;T | snv | 1 | |||||
| rs4319131 | 8 | 118935412 | intron variant | A/G | snv | 0.33 | 1 | ||||
| rs6415470 | 8 | 118942872 | intron variant | G/A | snv | 0.67 | 1 | ||||
| rs6469788 | 8 | 118940511 | intron variant | A/C;T | snv | 1 | |||||
| rs6469789 | 8 | 118948422 | intron variant | C/A;G;T | snv | 1 | |||||
| rs7463176 | 8 | 118945386 | intron variant | A/C;G | snv | 1 | |||||
| rs7464496 | 8 | 118942603 | intron variant | T/C | snv | 0.60 | 1 |