Source: CLINVAR
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121908987 | 0.742 | 0.200 | 7 | 151576412 | missense variant | C/A;G;T | snv | 4.0E-06 | 6 | ||
| rs193922697 | 1.000 | 0.040 | 7 | 151576438 | missense variant | G/A;T | snv | 1.6E-05 | 2 | ||
| rs267606976 | 1.000 | 0.080 | 7 | 151564203 | missense variant | A/G | snv | 2 | |||
| rs121908989 | 0.882 | 0.080 | 7 | 151564199 | missense variant | T/A;C | snv | 4.0E-06 | 1 |