| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs776428407 | 1.000 | 0.120 | 7 | 27174194 | missense variant | C/A;T | snv | 4.3E-06; 4.3E-06 | 1 | ||
| rs1284683098 | 1.000 | 0.120 | 2 | 176093070 | synonymous variant | G/A | snv | 1 | |||
| rs907715 | 0.752 | 0.520 | 4 | 122613898 | intron variant | C/T | snv | 0.35 | 11 | ||
| rs12508721 | 0.742 | 0.360 | 4 | 122623509 | intron variant | C/T | snv | 0.24 | 11 | ||
| rs2055979 | 0.827 | 0.320 | 4 | 122619586 | intron variant | C/A | snv | 0.23 | 6 | ||
| rs153109 | 0.623 | 0.600 | 16 | 28507775 | intron variant | T/C | snv | 0.43 | 37 | ||
| rs17855750 | 0.695 | 0.480 | 16 | 28503907 | missense variant | A/C;T | snv | 6.4E-02; 4.0E-06 | 21 | ||
| rs6523 | 0.882 | 0.200 | 19 | 17821329 | missense variant | T/C | snv | 0.65 | 0.70 | 4 | |
| rs1003887 | 0.882 | 0.240 | 19 | 17816591 | 3 prime UTR variant | C/T | snv | 0.69 | 3 | ||
| rs1047233 | 0.925 | 0.200 | 19 | 17821381 | synonymous variant | T/A;C;G | snv | 0.30 | 0.37 | 2 | |
| rs2286663 | 0.925 | 0.200 | 19 | 17821480 | synonymous variant | C/T | snv | 0.10 | 7.3E-02 | 2 | |
| rs104894697 | 1.000 | 0.120 | 19 | 17816972 | missense variant | G/A;C | snv | 3.5E-04; 4.0E-06 | 1 | ||
| rs104894698 | 1.000 | 0.120 | 19 | 17816946 | missense variant | G/A | snv | 4.0E-06 | 2.1E-05 | 1 | |
| rs121912555 | 1.000 | 0.120 | 19 | 17816920 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs121912556 | 1.000 | 0.120 | 19 | 17816945 | missense variant | C/T | snv | 6.9E-04 | 2.7E-04 | 1 | |
| rs398122886 | 1.000 | 0.120 | 19 | 17817033 | stop gained | G/A | snv | 1.6E-05 | 7.0E-06 | 1 | |
| rs570837260 | 1.000 | 0.120 | 19 | 17821391 | missense variant | A/C | snv | 7.3E-04 | 5.5E-04 | 1 | |
| rs1562134961 | 0.776 | 0.320 | 6 | 78969879 | frameshift variant | A/- | delins | 13 | |||
| rs1057516033 | 0.807 | 0.400 | 10 | 75025250 | splice donor variant | G/A | snv | 9 | |||
| rs3757824 | 0.882 | 0.160 | 7 | 17296411 | non coding transcript exon variant | T/C;G | snv | 3 | |||
| rs1565573786 | 0.807 | 0.160 | 12 | 49091165 | stop gained | G/C;T | snv | 6 | |||
| rs1480612338 | 0.851 | 0.160 | 12 | 49090416 | missense variant | C/T | snv | 4.3E-06 | 4 | ||
| rs4758680 | 0.763 | 0.320 | 12 | 122170805 | intron variant | T/A;G | snv | 9 | |||
| rs7977932 | 0.763 | 0.320 | 12 | 122172836 | intron variant | C/G;T | snv | 10 | |||
| rs61752717 | 0.583 | 0.840 | 16 | 3243407 | missense variant | T/A;C | snv | 2.8E-04 | 72 |