| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
| rs34811474 | 1.000 | 0.040 | 4 | 25407216 | missense variant | G/A;T | snv | 0.15; 4.1E-06 | 8 | ||
| rs2145272 | 20 | 6645571 | intergenic variant | G/A;T | snv | 7 | |||||
| rs72681869 | 14 | 50188639 | missense variant | G/A;C | snv | 4.0E-06; 4.1E-03 | 6 | ||||
| rs11012732 | 0.882 | 0.080 | 10 | 21541175 | intron variant | A/G | snv | 0.31 | 3 | ||
| rs3751837 | 16 | 3533173 | 3 prime UTR variant | C/A;T | snv | 0.22 | 0.23 | 3 | |||
| rs41310284 | 10 | 100687890 | intergenic variant | C/A;T | snv | 3 | |||||
| rs2322622 | 13 | 59923197 | intron variant | T/A;C | snv | 2 |