Source: GWASCAT ×
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2607653 | 1.000 | 0.080 | 13 | 102066314 | intron variant | A/G | snv | 5.9E-02 | 2 | ||
| rs117168171 | 1.000 | 0.080 | 15 | 101854599 | downstream gene variant | C/G;T | snv | 2 | |||
| rs76043556 | 1.000 | 0.080 | 15 | 30060226 | intron variant | A/G | snv | 2.3E-02 | 2 | ||
| rs250567 | 1.000 | 0.080 | 16 | 23383078 | downstream gene variant | C/T | snv | 8.1E-02 | 2 | ||
| rs80147136 | 1.000 | 0.080 | 16 | 47050042 | intergenic variant | C/A | snv | 0.11 | 2 | ||
| rs73354145 | 1.000 | 0.080 | 17 | 81706393 | intron variant | C/T | snv | 5.1E-02 | 2 | ||
| rs57504626 | 1.000 | 0.080 | 19 | 19609590 | intron variant | C/T | snv | 0.10 | 2 | ||
| rs2823310 | 1.000 | 0.080 | 21 | 15497529 | intron variant | C/A | snv | 4.0E-02 | 2 | ||
| rs62210650 | 1.000 | 0.080 | 21 | 19649854 | intergenic variant | C/T | snv | 8.0E-02 | 2 | ||
| rs58847779 | 1.000 | 0.080 | 22 | 37736644 | intron variant | T/C | snv | 4.4E-02 | 2 |