| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10927875 | 1.000 | 0.040 | 1 | 15972817 | intron variant | C/T | snv | 0.29 | 3 | ||
| rs121917776 | 0.882 | 0.040 | 10 | 74112086 | missense variant | C/T | snv | 9.9E-05 | 7.0E-06 | 5 | |
| rs144683137 | 0.925 | 0.120 | 10 | 74074745 | missense variant | A/G;T | snv | 1.2E-05; 3.6E-05 | 2 | ||
| rs938335177 | 1.000 | 0.040 | 10 | 74043094 | synonymous variant | G/A | snv | 1 | |||
| rs1294156190 | 1.000 | 0.040 | 22 | 19880680 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs752863555 | 1.000 | 0.040 | 22 | 19919597 | missense variant | C/G;T | snv | 1.2E-05; 2.4E-05 | 1 | ||
| rs754065483 | 1.000 | 0.040 | 22 | 19918969 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs754916024 | 1.000 | 0.040 | 22 | 19878123 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs757239766 | 1.000 | 0.040 | 22 | 19880681 | missense variant | C/A;G;T | snv | 1.6E-05 | 1 | ||
| rs267607158 | 0.851 | 0.040 | 2 | 178740125 | stop gained | G/A | snv | 4 | |||
| rs1284689627 | 1.000 | 0.040 | 2 | 178550125 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs139517732 | 0.851 | 0.040 | 2 | 178802273 | missense variant | C/T | snv | 4.4E-05 | 1.4E-05 | 4 | |
| rs267607155 | 0.925 | 0.040 | 2 | 178782980 | missense variant | A/G;T | snv | 3 | |||
| rs1298494952 | 1.000 | 0.040 | 2 | 178789994 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
| rs879217756 | 1.000 | 0.040 | 2 | 178784108 | missense variant | C/T | snv | 1 | |||
| rs9268402 | 0.827 | 0.200 | 6 | 32373576 | intron variant | G/A | snv | 0.45 | 5 | ||
| rs199476301 | 0.851 | 0.040 | 15 | 63042874 | missense variant | G/A;T | snv | 4.0E-06 | 6 | ||
| rs199476317 | 0.827 | 0.080 | 15 | 63062263 | missense variant | G/A | snv | 6 | |||
| rs104894501 | 0.851 | 0.040 | 15 | 63044030 | stop gained | G/A;C;T | snv | 4.0E-06 | 5 | ||
| rs104894505 | 0.882 | 0.040 | 15 | 63044072 | missense variant | G/A | snv | 4 | |||
| rs199476314 | 0.882 | 0.040 | 15 | 63060930 | missense variant | T/G | snv | 4 | |||
| rs758264780 | 0.882 | 0.040 | 15 | 63044029 | frameshift variant | G/- | delins | 4 | |||
| rs1212453165 | 0.925 | 0.040 | 15 | 63043751 | missense variant | G/A | snv | 6.8E-06 | 3 | ||
| rs199476316 | 0.925 | 0.080 | 15 | 63062219 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 3 | |
| rs1071646 | 1.000 | 0.040 | 15 | 63059641 | splice region variant | C/A | snv | 0.67 | 0.65 | 1 |