Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1620977 | 1.000 | 0.040 | 1 | 72263459 | intron variant | A/G;T | snv | 3 | |||
| rs12124523 | 1.000 | 0.040 | 1 | 72155780 | intron variant | C/T | snv | 7.0E-02 | 2 | ||
| rs3128341 | 1 | 72284165 | intron variant | T/C | snv | 0.82 | 2 | ||||
| rs66495454 | 1 | 72282884 | upstream gene variant | -/TCC;TCCT | ins | 0.28 | 1 | ||||
| rs1026997 | 1 | 72050604 | intron variant | T/C | snv | 0.45 | 1 | ||||
| rs114030538 | 1 | 72122975 | intron variant | T/C | snv | 4.1E-02 | 1 | ||||
| rs1157072 | 1 | 72169229 | intron variant | A/G | snv | 3.6E-02 | 1 | ||||
| rs11576565 | 1 | 71649104 | intron variant | G/A | snv | 0.36 | 1 | ||||
| rs11587895 | 1 | 72146932 | intron variant | T/C | snv | 0.22 | 1 | ||||
| rs12128707 | 1 | 72122436 | intron variant | A/G | snv | 0.21 | 1 | ||||
| rs12130762 | 1 | 71687405 | intron variant | G/A | snv | 6.5E-02 | 1 | ||||
| rs12133604 | 1 | 72145196 | intron variant | G/T | snv | 0.41 | 1 | ||||
| rs12137231 | 1 | 72269775 | intron variant | T/C | snv | 0.35 | 1 | ||||
| rs12139692 | 1 | 71995699 | intron variant | C/T | snv | 7.4E-02 | 1 | ||||
| rs12143094 | 1 | 71639693 | intron variant | G/C | snv | 3.9E-02 | 1 | ||||
| rs12564885 | 1 | 71597627 | intron variant | A/T | snv | 0.24 | 1 | ||||
| rs1486091 | 1 | 72105681 | intron variant | C/T | snv | 0.55 | 1 | ||||
| rs17589603 | 1 | 72167202 | intron variant | A/G | snv | 7.4E-02 | 1 | ||||
| rs1870676 | 1 | 72279313 | intron variant | T/C | snv | 0.48 | 1 | ||||
| rs2016698 | 1 | 72096795 | intron variant | G/A | snv | 0.23 | 1 | ||||
| rs2821260 | 1 | 72088410 | intron variant | C/T | snv | 0.59 | 1 | ||||
| rs34305371 | 1 | 72267927 | intron variant | G/A | snv | 6.6E-02 | 1 | ||||
| rs4348675 | 1 | 72050034 | intron variant | T/C | snv | 9.0E-02 | 1 | ||||
| rs67474621 | 1 | 72112267 | intron variant | A/C;T | snv | 1 | |||||
| rs77944304 | 1 | 72117096 | intron variant | C/T | snv | 0.18 | 1 |