| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs780159 | 10 | 79147390 | intron variant | A/C;G | snv | 2 | |||||
| rs1815314 | 10 | 79169036 | intron variant | G/A;C;T | snv | 1 | |||||
| rs1250552 | 0.882 | 0.200 | 10 | 79298270 | intron variant | A/C;G | snv | 1 | |||
| rs753270 | 1.000 | 0.080 | 10 | 79205218 | intron variant | T/A;C | snv | 1 | |||
| rs34204798 | 1.000 | 0.080 | 10 | 79191374 | intron variant | G/-;GG;GGG;GGGG | delins | 1 | |||
| rs703972 | 1.000 | 0.080 | 10 | 79193069 | intron variant | G/A;C | snv | 1 | |||
| rs1782645 | 1.000 | 0.080 | 10 | 79288854 | intron variant | C/A;T | snv | 1 | |||
| rs703984 | 10 | 79181660 | intron variant | G/C;T | snv | 1 |