| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1805129 | 0.882 | 0.120 | 22 | 28734470 | synonymous variant | T/C | snv | 3.6E-02 | 4.0E-02 | 3 | |
| rs587780191 | 0.882 | 0.120 | 22 | 28699931 | missense variant | T/C;G | snv | 4.0E-06; 1.6E-05 | 3 | ||
| rs759920 | 0.882 | 0.120 | 19 | 10174102 | intron variant | A/G;T | snv | 3 | |||
| rs79722116 | 0.882 | 0.120 | 9 | 95107192 | synonymous variant | C/T | snv | 4.6E-04 | 2.0E-04 | 3 | |
| rs7727832 | 0.882 | 0.120 | 5 | 142611975 | intron variant | C/T | snv | 0.10 | 3 | ||
| rs1136905 | 0.882 | 0.120 | 6 | 32518660 | missense variant | T/A;C | snv | 4.2E-03 | 3 | ||
| rs4320932 | 0.882 | 0.120 | 11 | 2150371 | intron variant | T/C | snv | 0.19 | 3 | ||
| rs266851 | 0.882 | 0.120 | 19 | 50833083 | intron variant | C/T | snv | 0.20 | 3 | ||
| rs10098821 | 0.882 | 0.120 | 8 | 128546982 | intron variant | C/T | snv | 7.6E-02 | 3 | ||
| rs1516982 | 0.882 | 0.120 | 8 | 128521400 | intron variant | A/G | snv | 0.16 | 3 | ||
| rs873330 | 0.882 | 0.120 | 13 | 104807897 | intergenic variant | A/G | snv | 0.31 | 3 | ||
| rs147961867 | 0.882 | 0.120 | 16 | 30121998 | missense variant | T/C | snv | 5.6E-05 | 2.8E-05 | 3 | |
| rs28933370 | 0.882 | 0.120 | 17 | 39725125 | missense variant | A/G | snv | 7.0E-06 | 3 | ||
| rs7526063 | 0.882 | 0.120 | 1 | 236808698 | splice region variant | C/T | snv | 3.8E-02 | 5.6E-02 | 3 | |
| rs11683487 | 0.882 | 0.120 | 2 | 151286035 | intron variant | G/T | snv | 0.36 | 3 | ||
| rs869312774 | 0.925 | 0.160 | 16 | 23614019 | frameshift variant | T/- | delins | 3 | |||
| rs608995 | 0.882 | 0.120 | 11 | 101035002 | 3 prime UTR variant | A/T | snv | 0.27 | 3 | ||
| rs3976507 | 0.882 | 0.120 | 3 | 179239995 | 3 prime UTR variant | C/T | snv | 0.19 | 0.24 | 3 | |
| rs61755649 | 0.882 | 0.160 | 14 | 67885891 | missense variant | C/T | snv | 6.8E-05 | 4.9E-05 | 3 | |
| rs372038369 | 0.882 | 0.160 | 17 | 35101233 | missense variant | G/A;T | snv | 1.2E-05 | 1.4E-05 | 3 | |
| rs113954997 | 0.882 | 0.280 | 11 | 14294844 | missense variant | T/A;C | snv | 3 | |||
| rs13063604 | 0.882 | 0.120 | 3 | 128085887 | intron variant | G/A | snv | 0.23 | 3 | ||
| rs7650365 | 0.882 | 0.120 | 3 | 128115160 | intron variant | G/A | snv | 0.35 | 3 | ||
| rs9303542 | 0.882 | 0.120 | 17 | 48334138 | intron variant | A/G | snv | 0.34 | 3 | ||
| rs2228026 | 0.882 | 0.120 | 14 | 20395890 | synonymous variant | A/G | snv | 4.7E-02 | 3.8E-02 | 3 |