| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6519955 | 0.925 | 0.120 | 22 | 46025962 | regulatory region variant | G/T | snv | 0.50 | 1 | ||
| rs7071275 | 1.000 | 0.120 | 10 | 121662920 | regulatory region variant | C/T | snv | 0.19 | 1 | ||
| rs7291412 | 1.000 | 0.120 | 22 | 46063252 | intron variant | G/T | snv | 0.36 | 1 | ||
| rs8124695 | 0.925 | 0.120 | 20 | 40399796 | intergenic variant | C/A;T | snv | 1 | |||
| rs977987 | 1.000 | 0.120 | 16 | 75472695 | 3 prime UTR variant | G/A | snv | 0.52 | 1 | ||
| rs9951109 | 1.000 | 0.120 | 18 | 9762936 | intron variant | T/A;C | snv | 1 | |||
| rs2306022 | 0.851 | 0.160 | 15 | 68335825 | missense variant | C/T | snv | 6.6E-02 | 5.8E-02 | 1 | |
| rs1042704 | 1.000 | 0.120 | 14 | 22843385 | missense variant | G/A;C | snv | 0.16 | 1 |