| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104893877 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 59 | |||
| rs63751273 | 0.645 | 0.280 | 17 | 46010389 | missense variant | C/T | snv | 42 | |||
| rs104893878 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 21 | |||
| rs1289324472 | 0.716 | 0.400 | 1 | 155236354 | missense variant | T/C | snv | 1.4E-05 | 21 | ||
| rs77369218 | 0.807 | 0.160 | 1 | 155235726 | missense variant | T/A | snv | 7 | |||
| rs2306604 | 0.827 | 0.080 | 10 | 58388932 | intron variant | A/C;G;T | snv | 5 | |||
| rs1041833271 | 0.925 | 0.080 | 21 | 25975995 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
| rs12734374 | 1.000 | 0.080 | 1 | 155419060 | intron variant | A/T | snv | 3.4E-02 | 2 | ||
| rs35749011 | 0.925 | 0.080 | 1 | 155162560 | intergenic variant | G/A | snv | 1.1E-02 | 2 | ||
| rs777296100 | 0.925 | 0.080 | 4 | 89725318 | 3 prime UTR variant | -/TAA;TAAAA | ins | 2 | |||
| rs1342971994 | 1.000 | 0.080 | 4 | 89822344 | missense variant | C/T | snv | 1.4E-05 | 1 | ||
| rs7681440 | 1.000 | 0.080 | 4 | 89835399 | intron variant | C/A;G | snv | 1 | |||
| rs1330229174 | 0.925 | 0.080 | 4 | 89835568 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
| rs1446915570 | 0.925 | 0.080 | 14 | 73173623 | synonymous variant | A/T | snv | 4.0E-06 | 7.0E-06 | 2 | |
| rs104893875 | 0.742 | 0.120 | 4 | 89828170 | missense variant | C/T | snv | 4.0E-06 | 13 | ||
| rs377591051 | 0.851 | 0.080 | 6 | 162262651 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 4 | |
| rs80356771 | 0.776 | 0.160 | 1 | 155235196 | missense variant | G/A;T | snv | 7.2E-05; 4.0E-06 | 8 | ||
| rs33939927 | 0.708 | 0.120 | 12 | 40310434 | missense variant | C/A;G;T | snv | 4.0E-06; 1.2E-05 | 24 | ||
| rs7308720 | 0.790 | 0.120 | 12 | 40263898 | missense variant | C/A;G | snv | 4.0E-06; 8.7E-02 | 7 | ||
| rs421016 | 0.683 | 0.440 | 1 | 155235252 | missense variant | A/C;G | snv | 8.0E-06; 1.3E-03 | 30 | ||
| rs143624519 | 0.724 | 0.240 | 17 | 45991484 | missense variant | G/A;T | snv | 1.5E-03; 1.2E-05 | 17 | ||
| rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
| rs7133914 | 0.790 | 0.120 | 12 | 40309109 | missense variant | G/A;T | snv | 8.5E-02; 1.6E-05 | 7 | ||
| rs78973108 | 0.776 | 0.160 | 1 | 155237453 | missense variant | C/T | snv | 2.8E-05 | 4.2E-05 | 8 | |
| rs80356769 | 0.776 | 0.160 | 1 | 155235772 | missense variant | C/A | snv | 3.2E-05 | 7.0E-06 | 8 |