Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121909330 | 0.752 | 0.200 | 9 | 35065364 | missense variant | G/A;C;T | snv | 11 | |||
rs121909334 | 0.752 | 0.200 | 9 | 35065255 | missense variant | C/T | snv | 1.6E-05 | 10 | ||
rs387906789 | 0.742 | 0.200 | 9 | 35065352 | missense variant | G/A;C | snv | 4.0E-06 | 14 | ||
rs387906709 | 0.776 | 0.120 | X | 56565363 | missense variant | C/A;T | snv | 9 | |||
rs367543041 | 0.742 | 0.200 | 1 | 11022553 | missense variant | G/A;C | snv | 3.0E-05 | 15 | ||
rs80356715 | 0.807 | 0.120 | 1 | 11016874 | missense variant | C/G;T | snv | 8.0E-06; 2.2E-04 | 6 | ||
rs104893877 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 59 | |||
rs63750215 | 0.701 | 0.240 | 1 | 226885603 | missense variant | A/T | snv | 19 | |||
rs63749824 | 0.776 | 0.120 | 14 | 73170945 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 8 | ||
rs63750082 | 0.732 | 0.120 | 14 | 73192712 | missense variant | G/C;T | snv | 8.0E-06 | 13 | ||
rs63750083 | 0.732 | 0.160 | 14 | 73219177 | missense variant | C/A;T | snv | 13 | |||
rs63750231 | 0.689 | 0.160 | 14 | 73198100 | missense variant | A/C;G | snv | 23 | |||
rs63750900 | 0.763 | 0.160 | 14 | 73198067 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 9 | |
rs63751068 | 0.827 | 0.120 | 14 | 73186920 | missense variant | G/C;T | snv | 6 | |||
rs63751399 | 0.882 | 0.120 | 14 | 73171047 | missense variant | T/A;C | snv | 3 | |||
rs74315401 | 0.683 | 0.320 | 20 | 4699525 | missense variant | C/T | snv | 32 | |||
rs63749855 | 0.790 | 0.200 | 17 | 46014271 | missense variant | T/G | snv | 8 | |||
rs63750376 | 0.827 | 0.120 | 17 | 45996657 | missense variant | G/T | snv | 7 | |||
rs63750424 | 0.677 | 0.240 | 17 | 46024061 | missense variant | C/T | snv | 1.6E-05 | 30 | ||
rs63750512 | 0.827 | 0.160 | 17 | 46024010 | missense variant | G/A;C | snv | 1.2E-05 | 6 | ||
rs63750635 | 0.851 | 0.120 | 17 | 46014286 | missense variant | C/T | snv | 5 | |||
rs63750756 | 0.716 | 0.200 | 17 | 46010324 | missense variant | T/G | snv | 2.6E-05 | 23 | ||
rs63750959 | 0.827 | 0.200 | 17 | 45962351 | missense variant | G/A;T | snv | 6.0E-05 | 5 | ||
rs63751273 | 0.645 | 0.280 | 17 | 46010389 | missense variant | C/T | snv | 42 | |||
rs63751438 | 0.776 | 0.120 | 17 | 46010388 | missense variant | C/T | snv | 16 |