Source: CURATED
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1566650594 | 0.851 | 0.120 | 14 | 73206384 | splice acceptor variant | A/T | snv | 4 | |||
rs63749824 | 0.776 | 0.120 | 14 | 73170945 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 4 | ||
rs63749836 | 0.827 | 0.160 | 14 | 73192786 | missense variant | G/A | snv | 5 | |||
rs63750053 | 0.827 | 0.120 | 14 | 73192721 | missense variant | G/T | snv | 4 | |||
rs63750082 | 0.732 | 0.120 | 14 | 73192712 | missense variant | G/C;T | snv | 8.0E-06 | 4 | ||
rs63750083 | 0.732 | 0.160 | 14 | 73219177 | missense variant | C/A;T | snv | 4 | |||
rs63750231 | 0.689 | 0.160 | 14 | 73198100 | missense variant | A/C;G | snv | 5 | |||
rs63750306 | 0.701 | 0.320 | 14 | 73173663 | missense variant | A/C;G;T | snv | 1 | |||
rs63750450 | 0.851 | 0.120 | 14 | 73173571 | missense variant | A/G | snv | 4 | |||
rs63750526 | 0.776 | 0.160 | 14 | 73192832 | missense variant | C/A | snv | 4 | |||
rs63750590 | 0.790 | 0.120 | 14 | 73186860 | missense variant | A/G | snv | 4 | |||
rs63750900 | 0.763 | 0.160 | 14 | 73198067 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 4 | |
rs63751068 | 0.827 | 0.120 | 14 | 73186920 | missense variant | G/C;T | snv | 2 | |||
rs63751223 | 0.807 | 0.160 | 14 | 73219161 | missense variant | G/C | snv | 5 | |||
rs63751278 | 0.827 | 0.120 | 14 | 73173631 | missense variant | A/G | snv | 4 | |||
rs63751287 | 0.742 | 0.120 | 14 | 73192792 | missense variant | A/G;T | snv | 4 | |||
rs661 | 0.807 | 0.120 | 14 | 73217225 | missense variant | G/A;T | snv | 4.0E-06 | 4 |