Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10455872 | 0.662 | 0.320 | 6 | 160589086 | intron variant | A/G | snv | 4.3E-02 | 10 | ||
| rs74617384 | 0.925 | 0.080 | 6 | 160576086 | intron variant | A/G;T | snv | 5 | |||
| rs140570886 | 1.000 | 0.040 | 6 | 160591981 | intron variant | T/C | snv | 2.8E-02 | 3 | ||
| rs41272114 | 1.000 | 0.040 | 6 | 160585045 | splice donor variant | C/A;T | snv | 1.2E-05; 4.1E-02 | 2 | ||
| rs55730499 | 1.000 | 0.040 | 6 | 160584578 | intron variant | C/T | snv | 4.5E-02 | 2 | ||
| rs6926458 | 1.000 | 0.040 | 6 | 160598834 | intron variant | A/G;T | snv | 2 | |||
| rs73596816 | 1.000 | 0.040 | 6 | 160596331 | intron variant | G/A | snv | 3.6E-02 | 2 | ||
| rs7770628 | 1.000 | 0.040 | 6 | 160597142 | intron variant | C/T | snv | 0.63 | 2 | ||
| rs10755578 | 0.925 | 0.040 | 6 | 160548706 | intron variant | C/G | snv | 0.44 | 0.42 | 1 | |
| rs3798220 | 0.732 | 0.160 | 6 | 160540105 | missense variant | T/C | snv | 5.6E-02 | 3.1E-02 | 1 | |
| rs6415084 | 1.000 | 0.040 | 6 | 160559298 | intron variant | T/C | snv | 0.57 | 1 | ||
| rs7767084 | 0.925 | 0.040 | 6 | 160541471 | intron variant | T/C | snv | 0.13 | 1 |