Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10061788 | 1.000 | 0.040 | 5 | 88638889 | intron variant | G/A;T | snv | 2 | |||
| rs10514301 | 5 | 88643836 | intron variant | C/T | snv | 0.16 | 2 | ||||
| rs6882046 | 1.000 | 0.040 | 5 | 88673046 | non coding transcript exon variant | A/G | snv | 0.29 | 2 | ||
| rs10070734 | 5 | 88644208 | intron variant | T/A;C | snv | 1 | |||||
| rs35267052 | 5 | 88653300 | intron variant | T/C;G | snv | 1 | |||||
| rs3814424 | 5 | 88673135 | non coding transcript exon variant | C/T | snv | 0.21 | 1 |