Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2280141 | 1.000 | 0.040 | 10 | 122433665 | 3 prime UTR variant | T/G | snv | 0.56 | 3 | ||
| rs6585827 | 1.000 | 0.040 | 10 | 122406099 | intron variant | G/A | snv | 0.47 | 3 | ||
| rs10510110 | 0.925 | 0.120 | 10 | 122432914 | 3 prime UTR variant | T/C | snv | 0.56 | 2 | ||
| rs2421016 | 0.925 | 0.120 | 10 | 122407996 | intron variant | C/T | snv | 0.46 | 2 | ||
| rs1045216 | 1.000 | 0.040 | 10 | 122429681 | missense variant | A/G | snv | 0.68 | 0.69 | 1 | |
| rs10749466 | 1.000 | 0.040 | 10 | 122379288 | intron variant | A/G | snv | 0.32 | 1 | ||
| rs10788284 | 1.000 | 0.040 | 10 | 122390401 | intron variant | T/C | snv | 0.55 | 1 | ||
| rs10887149 | 1.000 | 0.040 | 10 | 122407488 | intron variant | G/A;C | snv | 1 | |||
| rs10887150 | 1.000 | 0.040 | 10 | 122421062 | non coding transcript exon variant | C/A | snv | 0.47 | 1 | ||
| rs10887151 | 1.000 | 0.040 | 10 | 122421250 | non coding transcript exon variant | C/T | snv | 0.45 | 1 | ||
| rs11200594 | 1.000 | 0.040 | 10 | 122379877 | intron variant | C/T | snv | 0.47 | 1 | ||
| rs11200595 | 1.000 | 0.040 | 10 | 122383113 | intron variant | T/A;C | snv | 1 | |||
| rs11200604 | 1.000 | 0.040 | 10 | 122388123 | intron variant | G/A | snv | 0.47 | 1 | ||
| rs11200629 | 1.000 | 0.040 | 10 | 122439069 | 3 prime UTR variant | A/G | snv | 0.47 | 1 | ||
| rs17103488 | 1.000 | 0.040 | 10 | 122394653 | intron variant | T/C | snv | 0.11 | 1 | ||
| rs17103522 | 1.000 | 0.040 | 10 | 122418363 | non coding transcript exon variant | T/C | snv | 0.11 | 1 | ||
| rs2292626 | 0.925 | 0.120 | 10 | 122427198 | intron variant | C/T | snv | 0.46 | 1 | ||
| rs2292627 | 1.000 | 0.040 | 10 | 122442149 | 3 prime UTR variant | T/G | snv | 0.11 | 1 | ||
| rs2421017 | 1.000 | 0.040 | 10 | 122388651 | intron variant | A/G | snv | 0.54 | 1 | ||
| rs2421018 | 1.000 | 0.040 | 10 | 122388748 | intron variant | A/G | snv | 0.31 | 1 | ||
| rs2421019 | 1.000 | 0.040 | 10 | 122391070 | intron variant | C/T | snv | 0.31 | 1 | ||
| rs2421020 | 1.000 | 0.040 | 10 | 122391446 | intron variant | G/C | snv | 0.31 | 1 | ||
| rs4146894 | 1.000 | 0.040 | 10 | 122395865 | intron variant | C/T | snv | 0.48 | 1 | ||
| rs4311997 | 1.000 | 0.040 | 10 | 122419783 | non coding transcript exon variant | C/T | snv | 0.47 | 1 | ||
| rs4565845 | 1.000 | 0.040 | 10 | 122399534 | intron variant | A/C | snv | 0.19 | 1 |