| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11263654 | 1.000 | 0.120 | 11 | 69423355 | upstream gene variant | C/T | snv | 0.11 | 1 | ||
| rs13376700 | 1.000 | 0.120 | 1 | 51011971 | intergenic variant | T/A | snv | 0.48 | 1 | ||
| rs7765284 | 1.000 | 0.120 | 6 | 85068104 | intergenic variant | C/A | snv | 0.13 | 1 | ||
| rs78971134 | 1.000 | 0.120 | 12 | 107258753 | intergenic variant | A/G | snv | 7.7E-02 | 1 | ||
| rs1492078 | 1.000 | 0.120 | 3 | 148697390 | upstream gene variant | T/C | snv | 0.50 | 1 | ||
| rs7913447 | 1.000 | 0.120 | 10 | 72232282 | intron variant | C/A;T | snv | 1 | |||
| rs1800645 | 1.000 | 0.120 | 8 | 90083245 | intron variant | A/G;T | snv | 1 | |||
| rs1944129 | 1.000 | 0.120 | 11 | 69639167 | upstream gene variant | C/G;T | snv | 1 | |||
| rs1057519973 | 1.000 | 0.120 | 8 | 73946733 | missense variant | T/A;G | snv | 1 | |||
| rs1057519974 | 1.000 | 0.120 | 8 | 73946734 | missense variant | A/T | snv | 1 | |||
| rs10211665 | 1.000 | 0.120 | 2 | 46298957 | intron variant | T/C | snv | 0.58 | 1 | ||
| rs11125068 | 1.000 | 0.120 | 2 | 46300677 | intron variant | A/G | snv | 0.62 | 1 | ||
| rs11684885 | 1.000 | 0.120 | 2 | 46306413 | intron variant | T/C;G | snv | 1 | |||
| rs17034950 | 1.000 | 0.120 | 2 | 46311655 | intron variant | G/A | snv | 0.25 | 1 | ||
| rs1867784 | 1.000 | 0.120 | 2 | 46307081 | intron variant | T/C | snv | 0.40 | 1 | ||
| rs1867785 | 1.000 | 0.120 | 2 | 46307199 | intron variant | A/G | snv | 0.52 | 1 | ||
| rs1867787 | 1.000 | 0.120 | 2 | 46298252 | intron variant | G/C;T | snv | 1 | |||
| rs2034327 | 1.000 | 0.120 | 2 | 46321901 | intron variant | G/C | snv | 0.59 | 1 | ||
| rs2044456 | 1.000 | 0.120 | 2 | 46319177 | intron variant | A/G | snv | 0.26 | 1 | ||
| rs2121266 | 1.000 | 0.120 | 2 | 46308785 | intron variant | C/A | snv | 0.61 | 1 | ||
| rs2346417 | 1.000 | 0.120 | 2 | 46301822 | intron variant | T/A | snv | 0.39 | 1 | ||
| rs4952818 | 1.000 | 0.120 | 2 | 46309917 | intron variant | C/T | snv | 0.39 | 1 | ||
| rs4953340 | 1.000 | 0.120 | 2 | 46320925 | intron variant | C/A;G | snv | 1 | |||
| rs4953345 | 1.000 | 0.120 | 2 | 46325462 | intron variant | T/A;C | snv | 1 | |||
| rs9973653 | 1.000 | 0.120 | 2 | 46320970 | intron variant | G/T | snv | 0.42 | 1 |