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 | |||
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 | |||
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 | ||
rs80356715 | 0.807 | 0.120 | 1 | 11016874 | missense variant | C/G;T | snv | 8.0E-06; 2.2E-04 | 6 | ||
rs1314736087 | 0.851 | 0.120 | 8 | 109575782 | frameshift variant | GA/- | delins | 4.0E-06 | 5 | ||
rs544706237 | 0.851 | 0.120 | 2 | 79121649 | missense variant | A/G;T | snv | 8.0E-06; 5.2E-05 | 5 | ||
rs63750053 | 0.827 | 0.120 | 14 | 73192721 | missense variant | G/T | snv | 5 | |||
rs63750635 | 0.851 | 0.120 | 17 | 46014286 | missense variant | C/T | snv | 5 | |||
rs747105516 | 0.851 | 0.120 | 7 | 56015139 | missense variant | T/C | snv | 4.0E-06 | 5 | ||
rs1189501362 | 0.882 | 0.120 | 3 | 119863583 | missense variant | G/A | snv | 7.0E-06 | 4 | ||
rs1205185774 | 0.882 | 0.120 | 14 | 77469161 | missense variant | C/T | snv | 4 |