| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2074192 | 0.827 | 0.160 | X | 15564667 | intron variant | C/T | snv | 0.40 | 9 | ||
| rs518147 | 0.807 | 0.200 | X | 114584109 | 5 prime UTR variant | C/A;G | snv | 7 | |||
| rs1414334 | 0.851 | 0.160 | X | 114903581 | intron variant | C/G | snv | 5 | |||
| rs12836771 | 0.882 | 0.080 | X | 114650913 | intron variant | A/G | snv | 0.12 | 4 | ||
| rs17276588 | 0.882 | 0.120 | X | 53557457 | intron variant | G/A | snv | 9.0E-02 | 4.2E-02 | 4 | |
| rs5945326 | 0.925 | 0.080 | X | 153634467 | regulatory region variant | A/G | snv | 0.25 | 2 | ||
| rs782618876 | 0.925 | 0.080 | X | 153935333 | missense variant | G/A | snv | 3.4E-05 | 1.9E-05 | 2 | |
| rs1324805 | 1.000 | 0.040 | X | 109719433 | intron variant | A/G | snv | 0.45 | 1 | ||
| rs738409 | 0.557 | 0.720 | 22 | 43928847 | missense variant | C/G | snv | 0.28 | 0.22 | 88 | |
| rs1232898090 | 0.637 | 0.600 | 22 | 46198429 | missense variant | G/C;T | snv | 4.0E-06; 4.0E-06 | 40 | ||
| rs1800206 | 0.641 | 0.640 | 22 | 46218377 | missense variant | C/G | snv | 4.3E-02 | 4.2E-02 | 35 | |
| rs2267443 | 0.882 | 0.120 | 22 | 41891450 | intron variant | A/G | snv | 0.67 | 5 | ||
| rs1007888 | 0.882 | 0.120 | 22 | 23898914 | non coding transcript exon variant | C/T | snv | 0.46 | 4 | ||
| rs3213445 | 0.851 | 0.120 | 22 | 50577409 | missense variant | T/C | snv | 0.12 | 8.9E-02 | 4 | |
| rs1052717 | 0.925 | 0.080 | 22 | 41885425 | intron variant | A/G | snv | 0.62 | 3 | ||
| rs470117 | 1.000 | 0.040 | 22 | 50571524 | missense variant | C/T | snv | 0.42 | 0.36 | 2 | |
| rs561005732 | 0.925 | 0.040 | 22 | 24627519 | missense variant | A/C;G | snv | 8.0E-06 | 2 | ||
| rs2269383 | 1.000 | 0.040 | 22 | 50574346 | missense variant | C/T | snv | 2.6E-02 | 3.6E-02 | 1 | |
| rs5750146 | 1.000 | 0.040 | 22 | 35660681 | 3 prime UTR variant | G/A | snv | 8.7E-02 | 1 | ||
| rs5999924 | 1.000 | 0.040 | 22 | 35660097 | 3 prime UTR variant | A/G;T | snv | 1 | |||
| rs496300 | 1.000 | 0.040 | 21 | 43359800 | intron variant | C/T | snv | 0.73 | 2 | ||
| rs2295490 | 0.724 | 0.320 | 20 | 388261 | missense variant | A/G;T | snv | 0.18; 4.0E-06 | 16 | ||
| rs1884613 | 0.807 | 0.200 | 20 | 44351775 | intron variant | C/A;G;T | snv | 7 | |||
| rs13038305 | 0.925 | 0.080 | 20 | 23629625 | intron variant | C/T | snv | 0.21 | 5 | ||
| rs1884614 | 0.882 | 0.080 | 20 | 44351879 | non coding transcript exon variant | C/T | snv | 0.18 | 5 |