Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs646776 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 10 | ||
| rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 8 | ||
| rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 8 | ||
| rs7528419 | 0.851 | 0.080 | 1 | 109274570 | 3 prime UTR variant | A/G | snv | 0.23 | 7 | ||
| rs4970834 | 0.925 | 0.160 | 1 | 109272258 | intron variant | C/T | snv | 0.17 | 0.21 | 6 | |
| rs660240 | 1 | 109275216 | 3 prime UTR variant | T/C | snv | 0.75 | 5 | ||||
| rs611917 | 1.000 | 0.040 | 1 | 109272630 | non coding transcript exon variant | A/G | snv | 0.28 | 0.32 | 4 | |
| rs10858082 | 1 | 109256099 | intron variant | G/A | snv | 0.48 | 3 | ||||
| rs17035665 | 1 | 109271097 | intron variant | C/T | snv | 0.19 | 3 | ||||
| rs3832016 | 1 | 109275536 | 3 prime UTR variant | -/T | ins | 0.74 | 3 | ||||
| rs4970833 | 1 | 109262024 | intron variant | G/A | snv | 0.36 | 3 | ||||
| rs57677983 | 1 | 109275536 | 3 prime UTR variant | C/A;G;T | snv | 1.1E-02 | 3 | ||||
| rs6657811 | 1 | 109264661 | intron variant | A/C;T | snv | 4.0E-06; 0.10 | 3 | ||||
| rs6689614 | 1 | 109264477 | synonymous variant | G/A;C | snv | 0.44 | 3 | ||||
| rs6698843 | 0.925 | 0.080 | 1 | 109264212 | synonymous variant | C/A;T | snv | 4.0E-06; 0.44 | 3 |