| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs149989682 | 0.790 | 0.240 | 16 | 2317763 | missense variant | T/A;C | snv | 2.3E-03 | 10 | ||
| rs117603931 | 0.882 | 0.080 | 16 | 2319591 | missense variant | C/T | snv | 5.7E-03 | 6.5E-03 | 4 | |
| rs146709251 | 0.882 | 0.080 | 16 | 2279070 | missense variant | G/A | snv | 4.3E-03 | 3.0E-03 | 3 | |
| rs533117495 | 0.827 | 0.200 | 7 | 87595783 | missense variant | C/T | snv | 8.0E-06 | 5 | ||
| rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 | |
| rs2066853 | 0.653 | 0.600 | 7 | 17339486 | missense variant | G/A | snv | 0.15 | 0.22 | 34 | |
| rs2515475 | 1.000 | 0.040 | 8 | 6530918 | intron variant | C/T | snv | 0.19 | 1 | ||
| rs78142040 | 1.000 | 0.040 | X | 2914730 | non coding transcript exon variant | C/T | snv | 1 | |||
| rs13402990 | 1.000 | 0.040 | 2 | 70231632 | intron variant | A/T | snv | 9.7E-03 | 1 | ||
| rs2592178 | 1.000 | 0.040 | 2 | 70245350 | intron variant | G/A | snv | 0.27 | 1 | ||
| rs7022797 | 0.882 | 0.120 | 9 | 88989548 | upstream gene variant | T/G | snv | 0.38 | 3 | ||
| rs10905928 | 1.000 | 0.040 | 10 | 11300924 | intron variant | C/A | snv | 0.21 | 1 | ||
| rs2277212 | 1.000 | 0.040 | 10 | 11257772 | synonymous variant | A/T | snv | 0.75 | 0.74 | 1 | |
| rs7068124 | 1.000 | 0.040 | 10 | 11023453 | intron variant | T/C;G | snv | 1 | |||
| rs3814634 | 1.000 | 0.040 | 10 | 11099442 | splice region variant | G/T | snv | 0.37 | 1 | ||
| rs2606345 | 0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 | 16 | ||
| rs1800972 | 0.708 | 0.440 | 8 | 6877901 | 5 prime UTR variant | C/G;T | snv | 0.79 | 16 | ||
| rs11362 | 0.742 | 0.360 | 8 | 6877877 | 5 prime UTR variant | C/T | snv | 0.43 | 0.40 | 13 | |
| rs1799946 | 0.732 | 0.360 | 8 | 6877909 | 5 prime UTR variant | C/T | snv | 0.36 | 0.41 | 13 | |
| 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 | ||
| rs6533485 | 1.000 | 0.040 | 4 | 110006407 | intron variant | G/C | snv | 0.61 | 1 | ||
| rs516651 | 1.000 | 0.040 | 1 | 231406910 | intron variant | C/T | snv | 0.15 | 1 | ||
| rs324420 | 0.637 | 0.440 | 1 | 46405089 | missense variant | C/A | snv | 0.24 | 0.26 | 48 |