| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11825659 | 0.925 | 0.080 | 11 | 133925624 | intron variant | A/G | snv | 0.12 | 4 | ||
| rs1869324 | 1.000 | 0.080 | 2 | 137469872 | intron variant | G/A | snv | 7.9E-02 | 1 | ||
| rs11558538 | 0.695 | 0.400 | 2 | 138002079 | missense variant | C/T | snv | 1.0E-01 | 8.4E-02 | 1 | |
| rs12489456 | 1.000 | 0.080 | 3 | 14459666 | intron variant | G/A;T | snv | 1 | |||
| rs3773165 | 1.000 | 0.080 | 3 | 14482762 | intron variant | G/A | snv | 0.20 | 1 | ||
| rs6716455 | 1.000 | 0.080 | 2 | 150269889 | intron variant | G/A | snv | 0.11 | 3 | ||
| rs12392447 | 1.000 | 0.080 | X | 154496001 | non coding transcript exon variant | A/G | snv | 1 | |||
| rs9458121 | 1.000 | 0.080 | 6 | 161101446 | non coding transcript exon variant | A/G | snv | 8.4E-02 | 1 | ||
| rs115460205 | 1.000 | 0.080 | 4 | 161890417 | intron variant | C/T | snv | 4.7E-02 | 3 | ||
| rs17536732 | 1.000 | 0.080 | 4 | 161903214 | intron variant | G/T | snv | 4.7E-02 | 3 | ||
| rs9847462 | 1.000 | 0.080 | 3 | 164840807 | intergenic variant | A/G | snv | 0.14 | 1 | ||
| rs2168784 | 1.000 | 0.080 | 3 | 164872151 | intergenic variant | C/T | snv | 0.24 | 3 | ||
| rs10211296 | 1.000 | 0.080 | 2 | 165633833 | intron variant | A/G | snv | 0.34 | 3 | ||
| rs1039002 | 0.851 | 0.080 | 6 | 165741969 | intron variant | G/A;T | snv | 1 | |||
| rs6778524 | 1.000 | 0.080 | 3 | 16814451 | intron variant | T/C | snv | 8.3E-02 | 1 | ||
| rs55768019 | 1.000 | 0.080 | 4 | 174106365 | intron variant | A/G | snv | 0.43 | 3 | ||
| rs6701037 | 1.000 | 0.080 | 1 | 175150943 | downstream gene variant | A/C;T | snv | 3 | |||
| rs6425323 | 1.000 | 0.080 | 1 | 175155900 | downstream gene variant | C/T | snv | 0.39 | 1 | ||
| rs1057302 | 1.000 | 0.080 | 1 | 175157287 | 3 prime UTR variant | A/G | snv | 0.38 | 1 | ||
| rs10913569 | 1.000 | 0.080 | 1 | 178548873 | non coding transcript exon variant | A/G;T | snv | 1 | |||
| rs12006002 | 1.000 | 0.080 | 9 | 18166901 | intron variant | C/T | snv | 0.30 | 1 | ||
| rs4384980 | 1.000 | 0.080 | 3 | 182741281 | upstream gene variant | A/C | snv | 0.48 | 1 | ||
| rs2727943 | 0.925 | 0.080 | 3 | 1856289 | intergenic variant | T/A;C | snv | 1 | |||
| rs1867877 | 1.000 | 0.080 | 11 | 18705901 | missense variant | T/C | snv | 3.5E-02 | 4.2E-02 | 3 | |
| rs55702914 | 0.925 | 0.080 | 2 | 197349672 | intergenic variant | C/G | snv | 0.37 | 4 |