Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28645722 | 8 | 19945383 | intron variant | G/A;T | snv | 3 | |||||
| rs316 | 8 | 19960925 | missense variant | C/A;T | snv | 0.13; 4.0E-06 | 3 | ||||
| rs320 | 0.827 | 0.200 | 8 | 19961566 | intron variant | T/A;G | snv | 3 | |||
| rs3200218 | 8 | 19966560 | 3 prime UTR variant | A/G;T | snv | 3 | |||||
| rs3208305 | 1.000 | 0.080 | 8 | 19966137 | 3 prime UTR variant | A/T | snv | 0.36 | 3 | ||
| rs326 | 8 | 19961928 | intron variant | A/G | snv | 0.37 | 3 | ||||
| rs3289 | 8 | 19965681 | 3 prime UTR variant | T/C | snv | 4.0E-02 | 3 | ||||
| rs331 | 8 | 19962894 | intron variant | G/A | snv | 0.30 | 3 | ||||
| rs343 | 1.000 | 0.080 | 8 | 19953276 | intron variant | C/A | snv | 9.8E-02 | 8.1E-02 | 3 | |
| rs3779788 | 8 | 19945582 | intron variant | C/T | snv | 0.11 | 3 | ||||
| rs3916027 | 8 | 19967357 | downstream gene variant | G/A | snv | 0.31 | 3 | ||||
| rs4921683 | 8 | 19967557 | downstream gene variant | T/A | snv | 0.14 | 3 | ||||
| rs4922115 | 8 | 19965319 | 3 prime UTR variant | G/A | snv | 0.15 | 0.14 | 3 | |||
| rs6999612 | 8 | 19945573 | intron variant | T/C | snv | 7.8E-02 | 3 | ||||
| rs7000460 | 8 | 19946291 | intron variant | A/C | snv | 7.9E-02 | 3 | ||||
| rs7009128 | 8 | 19930017 | intron variant | T/C | snv | 0.10 | 3 | ||||
| rs7016529 | 8 | 19949120 | intron variant | T/C | snv | 8.4E-02 | 3 | ||||
| rs9644636 | 8 | 19967385 | downstream gene variant | T/A;G | snv | 3 | |||||
| rs10099160 | 8 | 19964304 | intron variant | T/G | snv | 0.20 | 2 | ||||
| rs15285 | 1.000 | 0.040 | 8 | 19967156 | 3 prime UTR variant | C/T | snv | 0.36 | 1 |