| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2236661 | 1.000 | 0.040 | 11 | 118628678 | intron variant | C/G | snv | 0.24 | 0.20 | 1 | |
| rs494560 | 1.000 | 0.040 | 11 | 118650844 | non coding transcript exon variant | A/G | snv | 0.57 | 1 | ||
| rs4774756 | 1.000 | 0.040 | 15 | 55254859 | intron variant | A/C | snv | 0.66 | 1 | ||
| rs1048771 | 1.000 | 0.040 | 1 | 46278228 | synonymous variant | C/A;T | snv | 4.0E-06; 0.15 | 1 | ||
| rs6062302 | 0.882 | 0.040 | 20 | 63689615 | synonymous variant | T/C | snv | 0.74 | 0.81 | 1 | |
| rs115303435 | 1.000 | 0.040 | 20 | 63694806 | missense variant | G/A | snv | 3.2E-03 | 1.1E-03 | 1 | |
| rs1058319 | 1.000 | 0.040 | 20 | 63743036 | 3 prime UTR variant | C/A;T | snv | 0.21 | 1 | ||
| rs12433985 | 1.000 | 0.040 | 14 | 22780330 | non coding transcript exon variant | A/G | snv | 0.36 | 1 | ||
| rs12436190 | 1.000 | 0.040 | 14 | 22788107 | intron variant | A/G | snv | 0.30 | 1 | ||
| rs12888930 | 1.000 | 0.040 | 14 | 22779374 | intron variant | C/T | snv | 0.32 | 1 | ||
| rs2065134 | 1.000 | 0.040 | 14 | 22788980 | intron variant | T/C;G | snv | 1 | |||
| rs1197458016 | 1.000 | 0.040 | 9 | 15466782 | missense variant | T/C | snv | 1 | |||
| rs1336268032 | 1.000 | 0.040 | 6 | 159692718 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs10842893 | 1.000 | 0.040 | 12 | 27269953 | intron variant | C/T | snv | 7.1E-02 | 1 | ||
| rs547275481 | 1.000 | 0.040 | 19 | 1621886 | missense variant | C/T | snv | 4.2E-05 | 1 | ||
| rs781754593 | 1.000 | 0.040 | 1 | 12202039 | missense variant | A/G | snv | 4.2E-06 | 1 | ||
| rs3212112 | 1.000 | 0.040 | 14 | 103699345 | intron variant | A/C | snv | 7.1E-03 | 2.2E-02 | 1 | |
| rs3770502 | 1.000 | 0.040 | 2 | 216180336 | intron variant | C/T | snv | 0.12 | 1 | ||
| rs828704 | 1.000 | 0.040 | 2 | 216128888 | intron variant | C/A | snv | 0.81 | 1 | ||
| rs6519265 | 1.000 | 0.040 | 22 | 41629346 | intron variant | A/G | snv | 1 | |||
| rs5019252 | 1.000 | 0.040 | 20 | 63746996 | synonymous variant | C/T | snv | 0.34 | 0.30 | 1 | |
| rs3761121 | 1.000 | 0.040 | 20 | 63711343 | intron variant | T/C | snv | 0.10 | 1 | ||
| rs4635969 | 0.827 | 0.160 | 5 | 1308437 | downstream gene variant | G/A;T | snv | 2 | |||
| rs34988193 | 1.000 | 0.040 | 15 | 64943580 | missense variant | A/G | snv | 0.31 | 0.28 | 2 | |
| rs10464870 | 0.882 | 0.040 | 8 | 129465577 | intron variant | C/T | snv | 0.80 | 2 |