| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3751624 | 1.000 | 0.120 | 15 | 52282973 | intron variant | C/T | snv | 0.20 | 2 | ||
| rs2853502 | 1.000 | 0.200 | MT | 13276 | missense variant | A/C;G;T | snv | 2 | |||
| rs1160535157 | X | 120449056 | stop gained | G/C | snv | 1 | |||||
| rs773223321 | 4 | 89935190 | missense variant | G/A | snv | 1.6E-05 | 1 | ||||
| rs375090109 | 6 | 42722120 | missense variant | C/A;G | snv | 4.0E-06; 2.4E-05 | 1 | ||||
| rs735286 | 6 | 43776884 | non coding transcript exon variant | C/T | snv | 0.23 | 1 |