| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs199474714 | 0.925 | 0.080 | 1 | 154173113 | missense variant | C/T | snv | 4 | |||
| rs772816537 | 1.000 | 0.080 | 1 | 154173179 | missense variant | G/A | snv | 8.0E-06 | 3 | ||
| rs121964852 | 0.851 | 0.080 | 1 | 154172971 | missense variant | C/T | snv | 2 | |||
| rs80358247 | 0.882 | 0.080 | 1 | 154191993 | missense variant | A/C | snv | 4.0E-06 | 2 | ||
| rs1051226 | 1 | 154157607 | 3 prime UTR variant | G/A | snv | 1 | |||||
| rs121964853 | 0.925 | 0.080 | 1 | 154176194 | missense variant | G/C;T | snv | 1 | |||
| rs121964854 | 0.882 | 0.080 | 1 | 154172972 | missense variant | G/A;C | snv | 1 | |||
| rs199474713 | 1.000 | 0.080 | 1 | 154176220 | missense variant | C/G | snv | 1 | |||
| rs1468885028 | 1.000 | 0.080 | 1 | 154172960 | missense variant | T/G | snv | 4.0E-06 | 1 |