Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5848 | 0.708 | 0.120 | 17 | 44352876 | 3 prime UTR variant | C/T | snv | 0.41 | 17 | ||
rs63751438 | 0.776 | 0.120 | 17 | 46010388 | missense variant | C/T | snv | 16 | |||
rs63750082 | 0.732 | 0.120 | 14 | 73192712 | missense variant | G/C;T | snv | 8.0E-06 | 13 | ||
rs63751287 | 0.742 | 0.120 | 14 | 73192792 | missense variant | A/G;T | snv | 13 | |||
rs80356726 | 0.763 | 0.120 | 1 | 11022352 | splice acceptor variant | G/A | snv | 4.0E-06 | 12 | ||
rs63750590 | 0.790 | 0.120 | 14 | 73186860 | missense variant | A/G | snv | 10 | |||
rs767543900 | 0.790 | 0.120 | 17 | 45971879 | missense variant | A/C;G | snv | 4.0E-06 | 10 | ||
rs387906709 | 0.776 | 0.120 | X | 56565363 | missense variant | C/A;T | snv | 9 | |||
rs1223904774 | 0.790 | 0.120 | 21 | 25891772 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 8 | |
rs34015634 | 0.851 | 0.120 | 12 | 40340380 | missense variant | T/C | snv | 3.2E-05 | 1.4E-05 | 8 | |
rs63749824 | 0.776 | 0.120 | 14 | 73170945 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 8 | ||
rs63750570 | 0.827 | 0.120 | 17 | 46018629 | missense variant | G/A | snv | 8 | |||
rs63750376 | 0.827 | 0.120 | 17 | 45996657 | missense variant | G/T | snv | 7 | |||
rs63750416 | 0.851 | 0.120 | 17 | 46010373 | missense variant | A/C | snv | 7 | |||
rs80356730 | 0.807 | 0.120 | 1 | 11022418 | missense variant | A/G | snv | 8.0E-06 | 7 | ||
rs142444896 | 0.807 | 0.120 | 7 | 56106409 | missense variant | G/A | snv | 9.3E-03 | 7.5E-03 | 6 | |
rs387906711 | 0.807 | 0.120 | X | 56565389 | missense variant | C/A;T | snv | 6.6E-06 | 6 | ||
rs63751068 | 0.827 | 0.120 | 14 | 73186920 | missense variant | G/C;T | snv | 6 | |||
rs63751278 | 0.827 | 0.120 | 14 | 73173631 | missense variant | A/G | snv | 6 | |||
rs63751294 | 0.827 | 0.120 | 17 | 44352404 | stop gained | C/T | snv | 8.0E-06 | 6 | ||
rs661 | 0.807 | 0.120 | 14 | 73217225 | missense variant | G/A;T | snv | 4.0E-06 | 6 | ||
rs769446 | 0.882 | 0.120 | 19 | 44905371 | upstream gene variant | T/C | snv | 7.0E-02 | 6 | ||
rs775129479 | 0.851 | 0.120 | 16 | 1791387 | missense variant | G/A;C;T | snv | 1.6E-05; 8.1E-06; 8.1E-06 | 6 | ||
rs781587642 | 0.851 | 0.120 | 2 | 219250557 | missense variant | G/A;C | snv | 2.0E-05 | 6 | ||
rs80356715 | 0.807 | 0.120 | 1 | 11016874 | missense variant | C/G;T | snv | 8.0E-06; 2.2E-04 | 6 |