| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11656696 | 0.882 | 0.040 | 17 | 10130362 | intron variant | C/A | snv | 0.36 | 5 | ||
| rs747058633 | 0.925 | 0.040 | 14 | 102083827 | missense variant | T/C | snv | 4.0E-06 | 2.8E-05 | 2 | |
| rs781662103 | 1.000 | 0.040 | 11 | 102797141 | synonymous variant | A/G | snv | 8.0E-06 | 1.4E-05 | 1 | |
| rs1799750 | 0.592 | 0.760 | 11 | 102799765 | intron variant | C/- | delins | 0.50 | 48 | ||
| rs2472493 | 0.851 | 0.040 | 9 | 104933567 | downstream gene variant | G/A | snv | 0.61 | 5 | ||
| rs576499843 | 0.882 | 0.040 | 1 | 107617607 | missense variant | A/C;G | snv | 8.0E-06 | 7.0E-06 | 3 | |
| rs1466441587 | 0.882 | 0.040 | 1 | 107874935 | missense variant | G/A | snv | 7.0E-06 | 3 | ||
| rs2801219 | 0.882 | 0.040 | 1 | 107959790 | intron variant | C/A | snv | 0.62 | 3 | ||
| rs757228 | 0.925 | 0.120 | 19 | 1101993 | upstream gene variant | A/G | snv | 0.54 | 2 | ||
| rs145437203 | 1.000 | 0.040 | 5 | 111092362 | missense variant | T/C | snv | 7.2E-03; 4.0E-06 | 7.6E-03 | 1 | |
| rs10038177 | 0.925 | 0.040 | 5 | 111100751 | intron variant | C/T | snv | 0.53 | 0.54 | 3 | |
| rs11241095 | 0.925 | 0.040 | 5 | 111103810 | missense variant | A/C;G | snv | 0.33 | 3 | ||
| rs34595252 | 0.925 | 0.040 | 5 | 111119021 | missense variant | A/G | snv | 4.3E-03 | 4.5E-03 | 2 | |
| rs13186912 | 1.000 | 0.040 | 5 | 111121006 | synonymous variant | A/T | snv | 0.33 | 0.26 | 2 | |
| rs4938723 | 0.574 | 0.680 | 11 | 111511840 | intron variant | T/C | snv | 0.32 | 60 | ||
| rs197388 | 0.925 | 0.040 | 1 | 111754860 | non coding transcript exon variant | A/T | snv | 0.27 | 2 | ||
| rs1052990 | 0.882 | 0.040 | 7 | 116508316 | 3 prime UTR variant | T/C;G | snv | 3 | |||
| rs17588172 | 0.925 | 0.040 | 7 | 116513961 | intergenic variant | T/G | snv | 0.35 | 2 | ||
| rs4236601 | 0.882 | 0.040 | 7 | 116522675 | upstream gene variant | G/A | snv | 0.28 | 4 | ||
| rs3801994 | 1.000 | 0.040 | 7 | 116550415 | intron variant | G/A | snv | 7.0E-02 | 1 | ||
| rs185815146 | 1.000 | 0.040 | 10 | 116864069 | intron variant | G/A | snv | 2.9E-03 | 1 | ||
| rs1927911 | 0.658 | 0.640 | 9 | 117707776 | intron variant | A/G | snv | 0.62 | 28 | ||
| rs12377632 | 0.827 | 0.120 | 9 | 117710452 | intron variant | T/A;C | snv | 5 | |||
| rs2149356 | 0.742 | 0.360 | 9 | 117711921 | intron variant | T/G | snv | 0.54 | 14 | ||
| rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 |