| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs111505097 | 1.000 | 0.160 | 2 | 189008943 | missense variant | G/A;T | snv | 1 | |||
| rs112456072 | 1.000 | 0.160 | 2 | 189008961 | missense variant | G/A | snv | 1 | |||
| rs112978464 | 1.000 | 0.160 | 2 | 189004136 | missense variant | G/A | snv | 1 | |||
| rs113485686 | 1.000 | 0.160 | 2 | 189001554 | missense variant | G/A | snv | 1 | |||
| rs121912913 | 1.000 | 0.160 | 2 | 189004302 | missense variant | G/A;T | snv | 1 | |||
| rs121912914 | 1.000 | 0.160 | 2 | 189006400 | missense variant | G/A;T | snv | 1 | |||
| rs121912915 | 1.000 | 0.160 | 2 | 189006965 | missense variant | G/T | snv | 1 | |||
| rs121912916 | 1.000 | 0.160 | 2 | 189006207 | missense variant | G/A | snv | 1 | |||
| rs121912917 | 1.000 | 0.160 | 2 | 189008952 | missense variant | G/A;T | snv | 1 | |||
| rs121912918 | 1.000 | 0.160 | 2 | 189008135 | missense variant | G/A;T | snv | 1 | |||
| rs121912919 | 1.000 | 0.160 | 2 | 188991678 | missense variant | G/A | snv | 1 | |||
| rs121912920 | 0.925 | 0.160 | 2 | 189002316 | missense variant | G/A | snv | 1 | |||
| rs121912921 | 1.000 | 0.160 | 2 | 188998693 | missense variant | G/A | snv | 1 | |||
| rs121912922 | 1.000 | 0.160 | 2 | 189004312 | missense variant | G/A;T | snv | 4.2E-06 | 1 | ||
| rs121912923 | 0.882 | 0.160 | 2 | 188996479 | missense variant | G/A;C;T | snv | 1 | |||
| rs121912924 | 1.000 | 0.160 | 2 | 189007546 | missense variant | G/A | snv | 1 | |||
| rs121912925 | 1.000 | 0.160 | 2 | 188999560 | missense variant | G/A;T | snv | 1 | |||
| rs121912926 | 1.000 | 0.160 | 2 | 188988099 | missense variant | G/A;C;T | snv | 1 | |||
| rs121912927 | 1.000 | 0.160 | 2 | 188990308 | missense variant | G/A;T | snv | 1 | |||
| rs1553507557 | 1.000 | 0.160 | 2 | 188991523 | missense variant | G/A | snv | 1 | |||
| rs587779419 | 1.000 | 0.160 | 2 | 188992923 | missense variant | G/A | snv | 1 | |||
| rs587779420 | 1.000 | 0.160 | 2 | 188988100 | missense variant | G/A;C | snv | 1 | |||
| rs587779427 | 1.000 | 0.160 | 2 | 188991005 | missense variant | G/T | snv | 1 | |||
| rs587779428 | 1.000 | 0.160 | 2 | 189006346 | missense variant | G/T | snv | 1 | |||
| rs587779431 | 1.000 | 0.160 | 2 | 189008108 | missense variant | G/A;T | snv | 1 |