| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs113993970 | 0.925 | 0.240 | 10 | 122506817 | stop gained | C/T | snv | 8.0E-06 | 3.5E-05 | 5 | |
| rs1143684 | 0.882 | 0.160 | 6 | 3010156 | missense variant | C/T | snv | 0.79 | 0.84 | 4 | |
| rs115199861 | 1.000 | 0.040 | 1 | 171670879 | non coding transcript exon variant | C/G;T | snv | 1 | |||
| rs11564148 | 0.851 | 0.080 | 12 | 40320099 | missense variant | T/A | snv | 0.30 | 0.27 | 4 | |
| rs115700680 | 1.000 | 0.040 | 1 | 171381070 | intergenic variant | T/G | snv | 1.9E-02 | 1 | ||
| rs115764752 | 1.000 | 0.040 | 1 | 171778066 | upstream gene variant | T/C | snv | 7.9E-03 | 1 | ||
| rs1157659 | 1.000 | 0.040 | 11 | 27736075 | intron variant | A/G | snv | 0.37 | 2 | ||
| rs115881343 | 1.000 | 0.040 | 19 | 44899959 | intron variant | C/G;T | snv | 2.9E-02 | 2 | ||
| rs116065238 | 1.000 | 0.040 | 1 | 171482283 | upstream gene variant | A/G | snv | 4.3E-03 | 1 | ||
| rs116237496 | 1.000 | 0.040 | 8 | 101033687 | upstream gene variant | T/C | snv | 4.0E-02 | 1 | ||
| rs11637611 | 0.851 | 0.160 | 15 | 72259371 | intron variant | C/T | snv | 0.63 | 4 | ||
| rs117070989 | 1.000 | 0.040 | 6 | 137490510 | downstream gene variant | C/A | snv | 8.3E-03 | 1 | ||
| rs117129097 | 1.000 | 0.040 | 12 | 128054737 | intron variant | C/G;T | snv | 1.9E-03 | 1 | ||
| rs117224174 | 1.000 | 0.040 | 6 | 114654261 | intergenic variant | G/A | snv | 2.2E-02 | 1 | ||
| rs117529438 | 1.000 | 0.040 | 12 | 64979216 | intron variant | C/T | snv | 3.4E-02 | 1 | ||
| rs117605016 | 1.000 | 0.040 | 12 | 129129840 | intron variant | C/A | snv | 9.9E-03 | 1 | ||
| rs117932393 | 1.000 | 0.040 | 9 | 106390428 | intron variant | C/T | snv | 8.4E-03 | 1 | ||
| rs11868035 | 0.763 | 0.200 | 17 | 17811787 | splice region variant | G/A | snv | 0.45 | 0.33 | 14 | |
| rs1187120 | 0.925 | 0.040 | 6 | 34182850 | intergenic variant | T/C | snv | 0.99 | 3 | ||
| rs11887120 | 0.882 | 0.080 | 2 | 25262866 | intron variant | C/T | snv | 0.45 | 4 | ||
| rs1206642175 | 0.925 | 0.080 | 6 | 151808263 | synonymous variant | G/A | snv | 7.0E-06 | 3 | ||
| rs121434610 | 0.882 | 0.120 | X | 21967312 | missense variant | G/A | snv | 3 | |||
| rs1216578110 | 1.000 | 0.040 | 21 | 25955652 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs121909668 | 0.790 | 0.120 | 16 | 31191418 | missense variant | C/A;G;T | snv | 1.2E-05 | 8 |