| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
| rs7096206 | 0.708 | 0.480 | 10 | 52771925 | upstream gene variant | G/A;C;T | snv | 17 | |||
| rs1800972 | 0.708 | 0.440 | 8 | 6877901 | 5 prime UTR variant | C/G;T | snv | 0.79 | 16 | ||
| rs149989682 | 0.790 | 0.240 | 16 | 2317763 | missense variant | T/A;C | snv | 2.3E-03 | 10 | ||
| rs315952 | 0.763 | 0.400 | 2 | 113132727 | missense variant | T/A;C | snv | 4.0E-06; 0.31 | 10 | ||
| rs1130866 | 0.827 | 0.160 | 2 | 85666618 | missense variant | G/A;C | snv | 0.50 | 9 | ||
| rs533117495 | 0.827 | 0.200 | 7 | 87595783 | missense variant | C/T | snv | 8.0E-06 | 5 | ||
| rs1322403577 | 0.882 | 0.120 | 10 | 79613818 | missense variant | T/C | snv | 4.0E-06 | 4 | ||
| rs3774934 | 0.851 | 0.080 | 4 | 102506319 | intron variant | A/C;G;T | snv | 4 | |||
| rs1059046 | 0.882 | 0.120 | 10 | 79559458 | missense variant | G/C;T | snv | 2.2E-05; 0.46 | 3 | ||
| rs761495176 | 0.882 | 0.080 | 5 | 143400263 | missense variant | T/C | snv | 1.7E-05 | 3 | ||
| rs7692976 | 1.000 | 0.040 | 4 | 109990411 | intron variant | A/G;T | snv | 2 | |||
| rs2298991 | 1.000 | 0.040 | 4 | 109970856 | intron variant | T/A;G | snv | 1 | |||
| rs4698803 | 1.000 | 0.040 | 4 | 109993271 | missense variant | A/G;T | snv | 0.85 | 1 | ||
| rs7068124 | 1.000 | 0.040 | 10 | 11023453 | intron variant | T/C;G | snv | 1 | |||
| rs78142040 | 1.000 | 0.040 | X | 2914730 | non coding transcript exon variant | C/T | snv | 1 | |||
| rs782230926 | 1.000 | 0.040 | 17 | 41734538 | missense variant | G/T | snv | 8.4E-06 | 7.0E-06 | 1 | |
| rs1320896171 | 0.882 | 0.120 | 17 | 2680294 | missense variant | C/T | snv | 7.0E-06 | 3 | ||
| rs1042689672 | 0.925 | 0.080 | 10 | 79557504 | missense variant | A/G | snv | 7.0E-06 | 2 | ||
| rs121434431 | 0.851 | 0.080 | 4 | 186083346 | missense variant | C/T | snv | 4.1E-04 | 5.2E-04 | 4 | |
| rs146709251 | 0.882 | 0.080 | 16 | 2279070 | missense variant | G/A | snv | 4.3E-03 | 3.0E-03 | 3 | |
| rs151139112 | 1.000 | 0.040 | 12 | 120322275 | missense variant | C/T | snv | 8.9E-04 | 3.2E-03 | 1 | |
| rs34568801 | 1.000 | 0.040 | 1 | 19975708 | missense variant | C/T | snv | 4.6E-03 | 4.3E-03 | 1 | |
| rs117603931 | 0.882 | 0.080 | 16 | 2319591 | missense variant | C/T | snv | 5.7E-03 | 6.5E-03 | 4 | |
| rs13402990 | 1.000 | 0.040 | 2 | 70231632 | intron variant | A/T | snv | 9.7E-03 | 1 |