| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2814778 | 0.763 | 0.360 | 1 | 159204893 | 5 prime UTR variant | T/C | snv | 0.25 | 11 | ||
| rs34599082 | 1 | 159205704 | missense variant | C/T | snv | 1.1E-02 | 9.9E-03 | 7 | |||
| rs12075 | 0.724 | 0.240 | 1 | 159205564 | missense variant | G/A | snv | 0.51 | 0.66 | 6 | |
| rs7550207 | 1 | 159205095 | intron variant | T/C | snv | 0.19 | 5 | ||||
| rs3027009 | 1 | 159204097 | intron variant | A/G | snv | 5.8E-02 | 2 | ||||
| rs3027001 | 1.000 | 0.040 | 1 | 159199673 | intron variant | C/G;T | snv | 2 | |||
| rs863006 | 1 | 159207958 | non coding transcript exon variant | G/A | snv | 0.56 | 1 | ||||
| rs13962 | 1 | 159205737 | missense variant | G/A | snv | 0.12 | 0.11 | 1 |