| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28362491 | 0.592 | 0.720 | 4 | 102500998 | non coding transcript exon variant | ATTG/- | delins | 56 | |||
| rs352140 | 0.630 | 0.680 | 3 | 52222681 | synonymous variant | C/A;G;T | snv | 2.0E-05; 0.49 | 42 | ||
| rs2232365 | 0.716 | 0.480 | X | 49259429 | intron variant | T/C | snv | 16 | |||
| rs749140677 | 0.752 | 0.240 | 12 | 47857185 | missense variant | G/A | snv | 8.0E-06 | 13 | ||
| rs16910526 | 0.742 | 0.280 | 12 | 10118488 | stop gained | A/C;G | snv | 6.2E-02 | 12 | ||
| rs2069727 | 0.763 | 0.320 | 12 | 68154443 | intron variant | T/A;C | snv | 9 | |||
| rs4693608 | 0.827 | 0.200 | 4 | 83320204 | intron variant | G/A;C | snv | 6 | |||
| rs6195 | 0.807 | 0.120 | 5 | 143399752 | missense variant | T/A;C | snv | 6 | |||
| rs37972 | 0.851 | 0.160 | 7 | 7967878 | 3 prime UTR variant | T/A;C | snv | 5 | |||
| rs1367967034 | 1.000 | 0.040 | 16 | 50707959 | splice region variant | A/G | snv | 4.0E-06 | 2 | ||
| rs17114808 | 0.925 | 0.040 | 10 | 102631528 | 3 prime UTR variant | C/A;G;T | snv | 2 | |||
| rs10737416 | 1.000 | 0.040 | 1 | 224887055 | intergenic variant | C/A;T | snv | 1 | |||
| rs17582214 | 1.000 | 0.040 | 9 | 119676531 | regulatory region variant | A/G;T | snv | 1 | |||
| rs2302217 | 1.000 | 0.040 | 19 | 498524 | synonymous variant | A/C;G | snv | 1.6E-05; 0.51 | 1 | ||
| rs337629 | 1.000 | 0.040 | 4 | 38633737 | intron variant | A/G;T | snv | 1 | |||
| rs4415345 | 1.000 | 0.040 | 8 | 7057895 | upstream gene variant | G/A;C | snv | 1 | |||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs1238539471 | 1.000 | 0.040 | 16 | 50710637 | synonymous variant | A/G | snv | 7.0E-06 | 2 | ||
| rs361525 | 0.562 | 0.760 | 6 | 31575324 | upstream gene variant | G/A | snv | 4.6E-02 | 62 | ||
| rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 46 | |
| rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
| rs3092936 | 1.000 | 0.040 | X | 136654046 | intron variant | T/C | snv | 8.9E-02 | 2 | ||
| rs3761549 | 0.724 | 0.480 | X | 49260888 | intron variant | G/A | snv | 9.6E-02 | 18 | ||
| rs6198 | 0.724 | 0.480 | 5 | 143278056 | 3 prime UTR variant | T/C | snv | 0.12 | 16 | ||
| rs4553808 | 0.672 | 0.320 | 2 | 203866282 | upstream gene variant | A/G;T | snv | 0.16 | 28 |