| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7048567 | 1.000 | 9 | 137009585 | synonymous variant | A/G | snv | 0.68 | 0.70 | 1 | ||
| rs78512431 | 1.000 | 21 | 43970856 | intron variant | T/A;C | snv | 0.10 | 1 | |||
| rs55797039 | 1.000 | 12 | 6363586 | missense variant | G/A;T | snv | 1.9E-02; 7.9E-05 | 1 | |||
| rs116502295 | 1.000 | 11 | 128462620 | intron variant | T/C | snv | 6.1E-03 | 7.1E-03 | 1 | ||
| rs75759941 | 0.925 | 0.080 | X | 38291789 | intron variant | T/C | snv | 7.5E-02 | 2 | ||
| rs10505380 | 1.000 | 8 | 120314234 | intron variant | A/G | snv | 0.14 | 1 | |||
| rs114830967 | 1.000 | 2 | 115820465 | intron variant | C/T | snv | 2.0E-02 | 1 | |||
| rs116264298 | 1.000 | 4 | 67496237 | intron variant | T/C | snv | 1.7E-02 | 1 | |||
| rs117451620 | 1.000 | 22 | 33873469 | intron variant | C/A | snv | 1.8E-02 | 1 | |||
| rs12118495 | 1.000 | 1 | 204077651 | intron variant | C/T | snv | 7.8E-02 | 1 | |||
| rs12232685 | 1.000 | 18 | 13437028 | intron variant | C/T | snv | 4.8E-02 | 1 | |||
| rs12539913 | 1.000 | 7 | 79143230 | intron variant | G/A | snv | 3.7E-02 | 1 | |||
| rs138288216 | 1.000 | 3 | 174250679 | intron variant | G/T | snv | 7.1E-03 | 1 | |||
| rs1394432 | 1.000 | 2 | 98279575 | intron variant | T/C | snv | 0.23 | 1 | |||
| rs139465532 | 1.000 | 20 | 8348184 | intron variant | C/G | snv | 6.8E-03 | 1 | |||
| rs139840509 | 1.000 | 18 | 6953581 | intron variant | G/A | snv | 1.1E-02 | 1 | |||
| rs140255439 | 1.000 | 17 | 2638960 | intron variant | C/T | snv | 6.3E-02 | 1 | |||
| rs142630661 | 1.000 | 11 | 71794579 | non coding transcript exon variant | C/G | snv | 1.3E-02 | 1 | |||
| rs142897541 | 1.000 | 2 | 192095144 | intron variant | C/T | snv | 1.6E-02 | 1 | |||
| rs146425640 | 1.000 | 11 | 19823052 | intron variant | A/C | snv | 2.8E-03 | 1 | |||
| rs149325996 | 1.000 | 18 | 79735872 | non coding transcript exon variant | G/A | snv | 1.0E-02 | 1 | |||
| rs150859230 | 1.000 | 1 | 216675108 | intron variant | C/T | snv | 1.4E-02 | 1 | |||
| rs151068302 | 1.000 | 9 | 26883048 | intron variant | C/T | snv | 6.1E-02 | 1 | |||
| rs1790634 | 1.000 | 18 | 36419450 | intron variant | G/A | snv | 0.58 | 1 | |||
| rs180822335 | 1.000 | 10 | 69950109 | intron variant | T/C | snv | 5.9E-03 | 1 |