Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6685859 | 1.000 | 0.040 | 1 | 97357213 | intron variant | G/C | snv | 0.45 | 2 | ||
| rs61789073 | 1.000 | 0.040 | 1 | 97938540 | intron variant | T/C | snv | 4.9E-02 | 2 | ||
| rs80289781 | 1.000 | 0.040 | 1 | 97980274 | intron variant | C/G;T | snv | 2 | |||
| rs11165867 | 1.000 | 0.040 | 1 | 97412512 | intron variant | C/T | snv | 0.16 | 1 | ||
| rs36025579 | 1.000 | 0.040 | 1 | 97337068 | intron variant | A/G | snv | 0.26 | 1 | ||
| rs76869799 | 1.000 | 0.040 | 1 | 97368969 | intron variant | C/G | snv | 2.6E-02 | 1 | ||
| rs4271249 | 1.000 | 0.040 | 1 | 97933063 | intron variant | G/T | snv | 0.45 | 1 |