| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
| rs901630 | 6 | 98091643 | intron variant | C/T | snv | 0.32 | 3 | ||||
| rs10872224 | 6 | 97987249 | intron variant | G/T | snv | 0.67 | 2 | ||||
| rs1144 | 7 | 105115908 | intron variant | T/C | snv | 0.31 | 2 | ||||
| rs2352974 | 3 | 49853180 | intron variant | C/A;T | snv | 2 | |||||
| rs8054299 | 16 | 53464743 | non coding transcript exon variant | C/A;G;T | snv | 2 |