| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs394563 | 1.000 | 0.120 | 6 | 149475878 | intron variant | T/C;G | snv | 1 | |||
| rs6102095 | 1.000 | 0.120 | 20 | 40692111 | upstream gene variant | G/A;C | snv | 1 | |||
| rs629535 | 1.000 | 0.120 | 8 | 69095703 | intron variant | C/T | snv | 0.19 | 1 | ||
| rs6496519 | 1.000 | 0.120 | 15 | 88694953 | intergenic variant | C/T | snv | 0.16 | 1 | ||
| rs7071275 | 1.000 | 0.120 | 10 | 121662920 | regulatory region variant | C/T | snv | 0.19 | 1 | ||
| rs7291412 | 1.000 | 0.120 | 22 | 46063252 | intron variant | G/T | snv | 0.36 | 1 | ||
| rs977987 | 1.000 | 0.120 | 16 | 75472695 | 3 prime UTR variant | G/A | snv | 0.52 | 1 | ||
| rs9951109 | 1.000 | 0.120 | 18 | 9762936 | intron variant | T/A;C | snv | 1 |