Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4925 | 0.677 | 0.560 | 10 | 104263031 | missense variant | C/A | snv | 0.25 | 0.23 | 28 | |
rs156697 | 0.672 | 0.560 | 10 | 104279427 | missense variant | A/G;T | snv | 0.35 | 25 | ||
rs104894201 | 0.763 | 0.280 | 11 | 111908934 | missense variant | T/C | snv | 12 | |||
rs58596362 | 0.827 | 0.280 | 1 | 156138613 | splice region variant | C/A;T | snv | 8.1E-06 | 7 | ||
rs1190613858 | 0.925 | 0.120 | 1 | 156139085 | synonymous variant | C/T | snv | 4.0E-06 | 3 | ||
rs3754334 | 0.925 | 0.040 | 1 | 16125272 | synonymous variant | G/A | snv | 0.28 | 0.24 | 2 | |
rs1136410 | 0.559 | 0.760 | 1 | 226367601 | missense variant | A/G | snv | 0.21 | 0.15 | 70 | |
rs1346044 | 0.708 | 0.440 | 8 | 31167138 | missense variant | T/C | snv | 0.24 | 0.23 | 23 | |
rs7278468 | 0.882 | 0.280 | 21 | 43168647 | upstream gene variant | T/A;G | snv | 3 | |||
rs25487 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 205 | |
rs13181 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 134 | ||
rs1052559 | 1.000 | 0.040 | 19 | 45351661 | stop gained | T/A;G | snv | 2 | |||
rs759412116 | 0.581 | 0.640 | 19 | 45352210 | missense variant | C/G;T | snv | 4.0E-06; 6.0E-05 | 55 | ||
rs79121622 | 0.827 | 0.080 | 16 | 67165833 | missense variant | G/A | snv | 3.3E-04 | 9.8E-05 | 5 | |
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 |