| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs60682848 | 0.790 | 0.200 | 1 | 156134838 | stop gained | C/T | snv | 7.0E-06 | 11 | ||
| rs61195471 | 0.827 | 0.160 | 1 | 156134496 | missense variant | G/A | snv | 6 | |||
| rs61444459 | 0.851 | 0.160 | 1 | 156137667 | missense variant | G/A;C | snv | 5 | |||
| rs74315380 | 0.851 | 0.080 | 1 | 201364366 | missense variant | G/A;C | snv | 5 | |||
| rs758264780 | 0.882 | 0.040 | 15 | 63044029 | frameshift variant | G/- | delins | 4 | |||
| rs867770797 | 0.851 | 0.200 | 4 | 147519875 | missense variant | G/A | snv | 8 | |||
| rs727503512 | 0.851 | 0.080 | 1 | 201363349 | missense variant | G/A;C;T | snv | 4.0E-06 | 5 | ||
| rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
| rs1393297693 | 1.000 | 0.040 | 6 | 43178806 | missense variant | G/A | snv | 4.0E-06 | 3 | ||
| rs761056344 | 0.925 | 0.080 | 6 | 118558994 | missense variant | C/G;T | snv | 4.0E-06; 3.2E-05 | 3 | ||
| rs1298494952 | 1.000 | 0.040 | 2 | 178789994 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
| rs104894501 | 0.851 | 0.040 | 15 | 63044030 | stop gained | G/A;C;T | snv | 4.0E-06 | 5 | ||
| rs746503158 | 1.000 | 0.040 | 10 | 133420125 | missense variant | A/G;T | snv | 8.0E-06; 4.0E-06 | 3 | ||
| rs386134243 | 0.708 | 0.360 | 1 | 156135967 | missense variant | C/A;T | snv | 4.0E-06 | 16 | ||
| rs199476301 | 0.851 | 0.040 | 15 | 63042874 | missense variant | G/A;T | snv | 4.0E-06 | 6 | ||
| rs45546039 | 0.732 | 0.120 | 3 | 38613781 | missense variant | C/A;T | snv | 4.1E-06 | 15 | ||
| rs1266360671 | 0.925 | 0.080 | 1 | 237270518 | missense variant | T/C | snv | 4.7E-06 | 3 | ||
| rs1212453165 | 0.925 | 0.040 | 15 | 63043751 | missense variant | G/A | snv | 6.8E-06 | 3 | ||
| rs137854618 | 0.742 | 0.120 | 3 | 38566426 | missense variant | C/A;T | snv | 8.0E-06 | 15 | ||
| rs730881071 | 1.000 | 0.040 | 19 | 55154158 | missense variant | G/A | snv | 8.0E-06 | 2 | ||
| rs59301204 | 0.925 | 0.080 | 1 | 156135956 | missense variant | G/A;C | snv | 1.2E-05 | 4 | ||
| rs397516695 | 0.882 | 0.040 | 2 | 219418869 | missense variant | T/A;C | snv | 5.5E-05 | 4 | ||
| rs138592977 | 1.000 | 0.040 | 1 | 156135968 | missense variant | G/A | snv | 5.6E-05 | 6.3E-05 | 3 | |
| rs121913002 | 0.851 | 0.160 | 2 | 219425727 | missense variant | C/A;G;T | snv | 6.5E-05; 5.6E-04 | 7 | ||
| rs146275785 | 0.925 | 0.040 | 10 | 20828531 | missense variant | G/A;T | snv | 7.2E-05; 2.7E-04 | 3 |