| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs9652601 | 1.000 | 0.080 | 16 | 11080508 | intron variant | G/A | snv | 0.34 | 1 | ||
| rs12599402 | 0.925 | 0.160 | 16 | 11096031 | intron variant | T/C | snv | 0.51 | 1 | ||
| rs8054198 | 1.000 | 0.080 | 16 | 10944503 | upstream gene variant | C/T | snv | 6.7E-02 | 1 | ||
| rs11865121 | 1.000 | 0.080 | 16 | 11072831 | intron variant | C/A | snv | 0.40 | 1 | ||
| rs6498160 | 1.000 | 0.080 | 16 | 11105590 | intron variant | T/C | snv | 0.51 | 1 | ||
| rs6498168 | 1.000 | 0.080 | 16 | 11141273 | intron variant | T/G | snv | 0.71 | 1 | ||
| rs17229044 | 1.000 | 0.120 | 16 | 10969079 | intron variant | C/T | snv | 0.16 | 1 | ||
| rs8061043 | 16 | 11067072 | intron variant | G/T | snv | 0.19 | 1 | ||||
| rs6498142 | 16 | 10987392 | intron variant | C/G | snv | 0.77 | 1 | ||||
| rs876476 | 16 | 11056391 | intron variant | G/A | snv | 0.26 | 1 | ||||
| rs12924112 | 1.000 | 0.120 | 16 | 11125863 | intron variant | T/A;G | snv | 1 | |||
| rs2041733 | 1.000 | 0.120 | 16 | 11135732 | intron variant | T/C;G | snv | 1 | |||
| rs62026377 | 16 | 11135271 | intron variant | G/T | snv | 0.23 | 1 |