| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
| rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
| rs53576 | 0.641 | 0.320 | 3 | 8762685 | intron variant | A/G;T | snv | 42 | |||
| rs6318 | 0.623 | 0.520 | X | 114731326 | missense variant | C/G;T | snv | 42 | |||
| rs698 | 0.724 | 0.240 | 4 | 99339632 | missense variant | T/A;C | snv | 0.35 | 20 | ||
| rs110402 | 0.790 | 0.120 | 17 | 45802681 | intron variant | G/A;C | snv | 12 | |||
| rs6923761 | 0.851 | 0.200 | 6 | 39066296 | missense variant | G/A;C | snv | 0.23; 4.0E-06 | 4 | ||
| rs6350 | 0.882 | 0.080 | 5 | 1443084 | missense variant | G/A;C | snv | 5.6E-02; 6.8E-05 | 3 | ||
| rs1015443 | 0.925 | 0.160 | 12 | 10908523 | missense variant | T/A;C | snv | 4.0E-06; 0.59 | 2 | ||
| rs11240 | 0.925 | 0.080 | 4 | 55453183 | 3 prime UTR variant | C/A;G | snv | 2 | |||
| rs10405681 | 1.000 | 0.080 | 19 | 3634021 | intron variant | C/A;T | snv | 1 | |||
| rs11250159 | 1.000 | 0.080 | 8 | 11729725 | intron variant | G/A;T | snv | 1 | |||
| rs1476592 | 1.000 | 0.080 | 19 | 3679742 | intron variant | A/G;T | snv | 1 | |||
| rs2074957 | 1.000 | 0.080 | 19 | 3653527 | synonymous variant | C/A;T | snv | 8.0E-06; 0.57 | 1 | ||
| rs4432372 | 1.000 | 0.080 | 19 | 3698844 | intron variant | A/G;T | snv | 1 | |||
| rs916264 | 1.000 | 0.080 | 22 | 36237790 | intron variant | A/C;T | snv | 1 | |||
| rs141973904 | 1.000 | 0.080 | 4 | 99341085 | intron variant | C/T | snv | 1.6E-02 | 1 | ||
| rs3756007 | 1.000 | 0.080 | 4 | 46389047 | 5 prime UTR variant | T/C | snv | 5.4E-02 | 2 | ||
| rs2066702 | 0.882 | 0.080 | 4 | 99307860 | missense variant | G/A | snv | 1.5E-02 | 5.9E-02 | 7 | |
| rs696217 | 0.662 | 0.640 | 3 | 10289773 | missense variant | G/T | snv | 8.8E-02 | 7.1E-02 | 32 | |
| rs2119183 | 1.000 | 0.080 | 4 | 46270789 | intron variant | G/A | snv | 7.6E-02 | 2 | ||
| rs56013859 | 0.925 | 0.080 | 2 | 238276865 | intron variant | T/C | snv | 0.11 | 2 | ||
| rs17153694 | 0.851 | 0.160 | 8 | 11730972 | intron variant | C/T | snv | 0.12 | 4 | ||
| rs11941860 | 1.000 | 0.080 | 4 | 46080161 | intron variant | C/T | snv | 0.12 | 2 | ||
| rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 |