| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1138690 | 1.000 | 0.120 | 4 | 3289674 | upstream gene variant | G/A;T | snv | 1 | |||
| rs12668183 | 1.000 | 0.120 | 7 | 16455781 | regulatory region variant | T/C | snv | 0.34 | 1 | ||
| rs7658462 | 1.000 | 0.120 | 4 | 3281695 | intergenic variant | C/T | snv | 0.16 | 1 | ||
| rs762847 | 1.000 | 0.120 | 4 | 2910336 | intron variant | A/G | snv | 0.54 | 1 | ||
| rs73786719 | 1.000 | 0.120 | 6 | 146716848 | intron variant | C/A | snv | 1.7E-02 | 3.3E-02 | 1 | |
| rs36117895 | 1.000 | 0.120 | 3 | 11358545 | missense variant | T/C | snv | 3.2E-02 | 3.9E-02 | 1 | |
| rs1170668763 | 1.000 | 0.120 | 17 | 42818395 | missense variant | T/A | snv | 7.0E-06 | 1 | ||
| rs756573441 | 1.000 | 0.120 | 7 | 134933359 | missense variant | A/G;T | snv | 4.2E-06 | 1 | ||
| rs1419046 | 1.000 | 0.120 | 4 | 2984322 | intron variant | T/A | snv | 0.39 | 1 | ||
| rs2471336 | 1.000 | 0.120 | 4 | 2995884 | intron variant | T/C | snv | 0.32 | 1 | ||
| rs2857845 | 1.000 | 0.120 | 4 | 3026386 | intron variant | A/T | snv | 0.11 | 1 | ||
| rs2960308 | 1.000 | 0.120 | 4 | 2989313 | intron variant | G/A | snv | 0.48 | 1 | ||
| rs4523977 | 1.000 | 0.120 | 17 | 41727098 | missense variant | G/A | snv | 0.23 | 0.18 | 1 | |
| rs10015979 | 1.000 | 0.120 | 4 | 3107715 | intron variant | A/G | snv | 0.30 | 1 | ||
| rs110501 | 1.000 | 0.120 | 4 | 3223751 | intron variant | T/C | snv | 0.47 | 1 | ||
| rs11731237 | 1.000 | 0.120 | 4 | 3150086 | intron variant | C/T | snv | 0.26 | 1 | ||
| rs1210554604 | 1.000 | 0.120 | 4 | 3131662 | missense variant | G/A | snv | 1 | |||
| rs2071655 | 1.000 | 0.120 | 4 | 3116389 | intron variant | T/A;G | snv | 1 | |||
| rs2269499 | 1.000 | 0.120 | 4 | 3237975 | intron variant | C/T | snv | 0.24 | 1 | ||
| rs2285086 | 1.000 | 0.120 | 4 | 3087532 | intron variant | A/G | snv | 0.48 | 1 | ||
| rs2298969 | 1.000 | 0.120 | 4 | 3184517 | intron variant | A/G;T | snv | 1 | |||
| rs2471347 | 1.000 | 0.120 | 4 | 3042708 | intron variant | G/A | snv | 0.68 | 1 | ||
| rs363066 | 1.000 | 0.120 | 4 | 3134226 | intron variant | T/A;G | snv | 1 | |||
| rs363096 | 1.000 | 0.120 | 4 | 3178294 | splice region variant | T/C | snv | 0.55 | 0.60 | 1 | |
| rs3856973 | 1.000 | 0.120 | 4 | 3078446 | intron variant | G/A;C | snv | 1 |