| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs34281605 | 1.000 | 0.080 | 15 | 38697473 | intron variant | G/A | snv | 0.26 | 1 | ||
| rs34356257 | 1.000 | 0.080 | 15 | 38697404 | intron variant | T/A;C | snv | 0.26 | 1 | ||
| rs35024396 | 1.000 | 0.080 | 15 | 38697569 | intron variant | G/A | snv | 0.25 | 1 | ||
| rs35102843 | 1.000 | 0.080 | 15 | 38695906 | intron variant | C/A | snv | 0.26 | 1 | ||
| rs35795311 | 1.000 | 0.080 | 15 | 38706468 | intron variant | C/G | snv | 0.24 | 1 | ||
| rs36094159 | 1.000 | 0.080 | 15 | 38706194 | intron variant | G/A | snv | 0.24 | 1 | ||
| rs7163869 | 1.000 | 0.080 | 15 | 38696190 | intron variant | G/C | snv | 0.26 | 1 | ||
| rs7165988 | 1.000 | 0.080 | 15 | 38696614 | non coding transcript exon variant | C/G;T | snv | 0.26; 4.0E-06 | 1 | ||
| rs7171233 | 1.000 | 0.080 | 15 | 38696559 | intron variant | T/A | snv | 0.26 | 0.26 | 1 | |
| rs7183893 | 1.000 | 0.080 | 15 | 38704780 | intron variant | A/C | snv | 0.23 | 1 | ||
| rs1800759 | 0.925 | 0.120 | 4 | 99144358 | intron variant | T/G | snv | 0.49 | 1 | ||
| rs12427267 | 1.000 | 0.080 | 12 | 91930196 | intergenic variant | A/G | snv | 0.49 | 1 | ||
| rs11558538 | 0.695 | 0.400 | 2 | 138002079 | missense variant | C/T | snv | 1.0E-01 | 8.4E-02 | 1 | |
| rs9458121 | 1.000 | 0.080 | 6 | 161101446 | non coding transcript exon variant | A/G | snv | 8.4E-02 | 1 | ||
| rs17754467 | 1.000 | 0.080 | 14 | 78156180 | intergenic variant | A/G | snv | 0.18 | 1 | ||
| rs3792686 | 1.000 | 0.080 | 4 | 4391341 | intron variant | T/C | snv | 0.41 | 1 | ||
| 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 | ||
| rs143894582 | 1.000 | 0.080 | 12 | 112469070 | intron variant | A/-;AA | delins | 1 | |||
| rs1451724 | 1.000 | 0.080 | 11 | 3835438 | intron variant | G/A | snv | 0.39 | 1 | ||
| rs12392447 | 1.000 | 0.080 | X | 154496001 | non coding transcript exon variant | A/G | snv | 1 | |||
| rs11922615 | 1.000 | 0.080 | 3 | 9416623 | intron variant | A/G | snv | 8.4E-02 | 1 | ||
| rs6443238 | 1.000 | 0.080 | 3 | 9407371 | intron variant | C/T | snv | 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 |