| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4898 | 0.672 | 0.520 | X | 47585586 | synonymous variant | T/C | snv | 0.46 | 0.46 | 25 | |
| rs762622506 | 0.925 | 0.080 | X | 40074459 | missense variant | C/A;T | snv | 6.1E-06 | 3 | ||
| rs867679539 | 0.925 | 0.080 | X | 130013883 | missense variant | A/C | snv | 3 | |||
| rs751661633 | 0.851 | 0.120 | 22 | 38984136 | missense variant | C/A | snv | 4.1E-06 | 6 | ||
| rs36600 | 0.827 | 0.080 | 22 | 29941597 | intron variant | T/C | snv | 0.78 | 5 | ||
| rs2051764 | 0.925 | 0.080 | 22 | 29965892 | intron variant | G/A;C | snv | 0.74 | 2 | ||
| rs36605 | 0.925 | 0.080 | 22 | 29944367 | intron variant | A/G;T | snv | 2 | |||
| rs737909 | 0.925 | 0.080 | 22 | 29992769 | non coding transcript exon variant | T/G | snv | 0.73 | 2 | ||
| rs1058024 | 1.000 | 0.040 | 22 | 45186979 | 3 prime UTR variant | G/A;C | snv | 1 | |||
| rs11089940 | 1.000 | 0.040 | 22 | 22155065 | intron variant | G/A | snv | 5.5E-02 | 1 | ||
| rs11090584 | 1.000 | 0.040 | 22 | 29853358 | intergenic variant | T/A;C | snv | 0.11 | 1 | ||
| rs11705386 | 1.000 | 0.040 | 22 | 27638385 | regulatory region variant | C/T | snv | 3.7E-02 | 1 | ||
| rs11913192 | 1.000 | 0.040 | 22 | 48447383 | upstream gene variant | G/A | snv | 8.3E-02 | 1 | ||
| rs12165516 | 1.000 | 0.040 | 22 | 47783584 | intron variant | A/G | snv | 0.12 | 1 | ||
| rs12484281 | 1.000 | 0.040 | 22 | 25787450 | intron variant | T/C | snv | 0.22 | 1 | ||
| rs12627929 | 1.000 | 0.040 | 22 | 30005238 | non coding transcript exon variant | A/G | snv | 9.4E-03 | 1 | ||
| rs12628523 | 1.000 | 0.040 | 22 | 25788238 | intron variant | T/C | snv | 2.6E-02 | 1 | ||
| rs13053400 | 1.000 | 0.040 | 22 | 17523132 | intron variant | G/A | snv | 5.4E-02 | 1 | ||
| rs132834 | 1.000 | 0.040 | 22 | 45158316 | intron variant | G/A;C | snv | 1 | |||
| rs132873 | 1.000 | 0.040 | 22 | 45170821 | intron variant | C/T | snv | 0.20 | 1 | ||
| rs132875 | 1.000 | 0.040 | 22 | 45171031 | 5 prime UTR variant | C/A;G | snv | 0.21 | 1 | ||
| rs132881 | 1.000 | 0.040 | 22 | 45171699 | non coding transcript exon variant | C/A | snv | 0.21 | 0.20 | 1 | |
| rs132883 | 1.000 | 0.040 | 22 | 45172630 | intron variant | G/T | snv | 0.20 | 1 | ||
| rs132884 | 1.000 | 0.040 | 22 | 45173105 | intron variant | A/G | snv | 0.20 | 1 | ||
| rs134009 | 1.000 | 0.040 | 22 | 27638589 | regulatory region variant | G/A | snv | 0.11 | 1 |