| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2306022 | 0.851 | 0.160 | 15 | 68335825 | missense variant | C/T | snv | 6.6E-02 | 5.8E-02 | 1 | |
| rs2912522 | 0.925 | 0.120 | 8 | 69080145 | intron variant | G/A | snv | 0.73 | 1 | ||
| rs629535 | 1.000 | 0.120 | 8 | 69095703 | intron variant | C/T | snv | 0.19 | 1 | ||
| rs977987 | 1.000 | 0.120 | 16 | 75472695 | 3 prime UTR variant | G/A | snv | 0.52 | 1 | ||
| rs4789939 | 0.925 | 0.120 | 17 | 78885621 | intron variant | T/A;C | snv | 1 | |||
| rs6496519 | 1.000 | 0.120 | 15 | 88694953 | intergenic variant | C/T | snv | 0.16 | 1 | ||
| rs4932194 | 0.925 | 0.120 | 15 | 88702008 | regulatory region variant | A/C;G;T | snv | 1 | |||
| rs9951109 | 1.000 | 0.120 | 18 | 9762936 | intron variant | T/A;C | snv | 1 |