| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1285576172 | 2 | 227284345 | missense variant | G/A | snv | 1 | |||||
| rs137876000 | 8 | 90042763 | missense variant | G/A | snv | 2.2E-04 | 1.1E-04 | 1 | |||
| rs755416212 | 1 | 97691775 | missense variant | C/T | snv | 1.2E-05 | 1 | ||||
| rs12118043 | 1 | 161677034 | non coding transcript exon variant | C/A | snv | 0.13 | 1 | ||||
| rs4657093 | 1 | 161723213 | intron variant | T/C | snv | 0.18 | 1 | ||||
| rs147121532 | 1 | 230316103 | 3 prime UTR variant | T/C | snv | 5.1E-03 | 1 |