Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs167511 | 1.000 | 0.040 | 10 | 4673284 | intron variant | A/G | snv | 6.3E-02 | 1 | ||
| rs313430 | 1.000 | 0.040 | 10 | 4669572 | intron variant | T/C | snv | 6.9E-02 | 1 | ||
| rs7916170 | 1.000 | 0.040 | 10 | 4679279 | intron variant | C/T | snv | 6.8E-02 | 1 | ||
| rs11598678 | 1.000 | 0.040 | 10 | 4657200 | non coding transcript exon variant | G/T | snv | 7.1E-02 | 1 | ||
| rs2647337 | 1.000 | 0.040 | 10 | 4655386 | intron variant | G/A;T | snv | 1 | |||
| rs1838239 | 1.000 | 0.040 | 10 | 4673826 | intron variant | C/T | snv | 0.17 | 1 | ||
| rs313455 | 1.000 | 0.040 | 10 | 4651821 | intron variant | T/C | snv | 0.22 | 1 | ||
| rs10508287 | 1.000 | 0.040 | 10 | 4658776 | intron variant | A/G | snv | 0.24 | 1 | ||
| rs1391511 | 1.000 | 0.040 | 10 | 4677604 | intron variant | A/G | snv | 0.46 | 1 | ||
| rs2165953 | 1.000 | 0.040 | 10 | 4674350 | intron variant | G/A | snv | 0.69 | 1 |