Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10222378 | 1.000 | 0.040 | 3 | 61063307 | intron variant | A/G;T | snv | 0.55 | 1 | ||
| rs13061562 | 1.000 | 0.040 | 3 | 61065916 | intron variant | T/C | snv | 0.45 | 1 | ||
| rs1965143 | 1.000 | 0.040 | 3 | 61062993 | intron variant | T/A;C | snv | 1 | |||
| rs7642017 | 1.000 | 0.040 | 3 | 61061729 | intron variant | C/T | snv | 0.61 | 1 | ||
| rs9850713 | 1.000 | 0.040 | 3 | 61062909 | intron variant | C/T | snv | 0.55 | 1 | ||
| rs9855931 | 1.000 | 0.040 | 3 | 61063887 | intron variant | C/G;T | snv | 1 | |||
| rs9869954 | 1.000 | 0.040 | 3 | 61062586 | intron variant | T/A;C | snv | 1 |