Source: GWASCAT ×
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 25 | |
| rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 23 | |||||
| rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 20 | |
| rs2294915 | 1.000 | 0.040 | 22 | 43945024 | intron variant | C/G;T | snv | 5 | |||
| rs3768321 | 1.000 | 0.080 | 1 | 39570256 | intron variant | G/T | snv | 0.14 | 5 | ||
| rs1811069 | 1.000 | 0.040 | 22 | 21627765 | upstream gene variant | T/A;G | snv | 4 |