Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
rs104894229 | 0.564 | 0.600 | 11 | 534289 | missense variant | C/A;G;T | snv | 73 | |||
rs28933979 | 0.587 | 0.600 | 18 | 31592974 | missense variant | G/A;C | snv | 1.0E-04 | 70 | ||
rs121913355 | 0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 | 42 | ||
rs397507520 | 0.658 | 0.520 | 12 | 112453279 | missense variant | G/C;T | snv | 39 | |||
rs80338796 | 0.667 | 0.480 | 3 | 12604200 | missense variant | G/A;C | snv | 4.0E-06 | 37 | ||
rs180177035 | 0.752 | 0.280 | 7 | 140801502 | missense variant | T/C | snv | 35 | |||
rs672601334 | 0.752 | 0.400 | 1 | 155904798 | missense variant | G/C | snv | 18 | |||
rs3218716 | 0.716 | 0.280 | 14 | 23425316 | missense variant | C/A;G;T | snv | 4.0E-06; 2.4E-05 | 17 | ||
rs730881014 | 0.776 | 0.360 | 1 | 155904494 | stop gained | A/C;G;T | snv | 15 | |||
rs753611141 | 0.827 | 0.280 | 9 | 136418847 | missense variant | G/A;T | snv | 2.4E-05; 4.0E-06 | 14 | ||
rs121918456 | 0.752 | 0.280 | 12 | 112473023 | missense variant | A/C;G | snv | 13 | |||
rs121918462 | 0.742 | 0.320 | 12 | 112450398 | missense variant | C/T | snv | 13 | |||
rs397507549 | 0.742 | 0.240 | 12 | 112489104 | missense variant | C/A;G | snv | 13 | |||
rs768643552 | 0.851 | 0.240 | 9 | 136418630 | missense variant | G/A;C | snv | 4.0E-06 | 13 | ||
rs104894201 | 0.763 | 0.280 | 11 | 111908934 | missense variant | T/C | snv | 12 | |||
rs121908987 | 0.742 | 0.200 | 7 | 151576412 | missense variant | C/A;G;T | snv | 4.0E-06 | 12 | ||
rs796051877 | 0.807 | 0.320 | 17 | 80110055 | splice region variant | G/A | snv | 4.0E-06 | 11 | ||
rs104894369 | 0.807 | 0.080 | 12 | 110914287 | missense variant | C/A;T | snv | 10 | |||
rs121913628 | 0.763 | 0.160 | 14 | 23424059 | missense variant | C/G;T | snv | 10 | |||
rs28935197 | 0.776 | 0.280 | X | 101398942 | missense variant | T/C | snv | 5.5E-06 | 10 | ||
rs3218713 | 0.763 | 0.160 | 14 | 23431468 | missense variant | C/A;T | snv | 10 | |||
rs587782958 | 0.790 | 0.120 | 11 | 47333552 | splice region variant | C/T | snv | 1.7E-05 | 10 | ||
rs111033560 | 0.807 | 0.040 | 6 | 118559037 | stop gained | T/G | snv | 1.6E-05 | 9 |