Source: GWASCAT ×
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs72804453 | 1.000 | 0.080 | 10 | 58827232 | intron variant | A/G | snv | 2.0E-02 | 2 | ||
| rs73354145 | 1.000 | 0.080 | 17 | 81706393 | intron variant | C/T | snv | 5.1E-02 | 2 | ||
| rs75298135 | 1.000 | 0.080 | 5 | 28184372 | intergenic variant | A/C | snv | 1.3E-02 | 2 | ||
| rs75639901 | 1.000 | 0.080 | 6 | 25667803 | intron variant | A/G | snv | 4.8E-02 | 2 | ||
| rs76043556 | 1.000 | 0.080 | 15 | 30060226 | intron variant | A/G | snv | 2.3E-02 | 2 | ||
| rs7810240 | 1.000 | 0.080 | 7 | 150387372 | intron variant | T/C;G | snv | 2 | |||
| rs80147136 | 1.000 | 0.080 | 16 | 47050042 | intergenic variant | C/A | snv | 0.11 | 2 | ||
| rs80333777 | 1.000 | 0.080 | 5 | 15524361 | intron variant | G/A;C;T | snv | 2 | |||
| rs9472719 | 1.000 | 0.080 | 6 | 46183649 | regulatory region variant | A/C | snv | 0.32 | 2 | ||
| rs34030778 | 1.000 | 0.080 | 8 | 1771328 | missense variant | C/T | snv | 2.8E-03 | 1.1E-02 | 2 |