Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | ||||
| rs10099160 | 8 | 19964304 | intron variant | T/G | snv | 0.20 | 2 | ||||
| rs328 | 0.732 | 0.440 | 8 | 19962213 | stop gained | C/G | snv | 9.2E-02 | 9.0E-02 | 7 | |
| rs268 | 0.637 | 0.480 | 8 | 19956018 | missense variant | A/G | snv | 1.3E-02 | 1.3E-02 | 4 | |
| rs316 | 8 | 19960925 | missense variant | C/A;T | snv | 0.13; 4.0E-06 | 3 | ||||
| rs3735964 | 1.000 | 0.080 | 8 | 19966534 | 3 prime UTR variant | C/A | snv | 9.1E-02 | 4 | ||
| rs1059507 | 1.000 | 0.080 | 8 | 19966452 | 3 prime UTR variant | C/T | snv | 0.15 | 3 | ||
| rs11570892 | 8 | 19966106 | 3 prime UTR variant | A/G;T | snv | 3 | |||||
| rs13702 | 0.925 | 0.160 | 8 | 19966981 | 3 prime UTR variant | T/A;C | 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 | ||
| rs3289 | 8 | 19965681 | 3 prime UTR variant | T/C | snv | 4.0E-02 | 3 | ||||
| rs4922115 | 8 | 19965319 | 3 prime UTR variant | G/A | snv | 0.15 | 0.14 | 3 | |||
| rs15285 | 1.000 | 0.040 | 8 | 19967156 | 3 prime UTR variant | C/T | snv | 0.36 | 1 | ||
| rs3916027 | 8 | 19967357 | downstream gene variant | G/A | snv | 0.31 | 3 | ||||
| rs4921683 | 8 | 19967557 | downstream gene variant | T/A | snv | 0.14 | 3 | ||||
| rs9644636 | 8 | 19967385 | downstream gene variant | T/A;G | snv | 3 |