Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121434568 | 0.568 | 0.560 | 7 | 55191822 | missense variant | T/A;G | snv | 73 | |||
rs1057519847 | 0.570 | 0.560 | 7 | 55191821 | missense variant | CT/AG | mnv | 72 | |||
rs1057519848 | 0.570 | 0.560 | 7 | 55191822 | missense variant | TG/GT | mnv | 72 | |||
rs121434569 | 0.581 | 0.520 | 7 | 55181378 | missense variant | C/T | snv | 2.8E-05 | 5.6E-05 | 70 | |
rs2227983 | 0.658 | 0.520 | 7 | 55161562 | missense variant | G/A;C;T | snv | 0.29 | 31 | ||
rs751295137 | 0.851 | 0.160 | 7 | 55152582 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 6 | |
rs760101437 | 0.851 | 0.160 | 7 | 55154018 | missense variant | G/A | snv | 3.2E-05 | 1.4E-05 | 6 | |
rs377444977 | 0.882 | 0.080 | 7 | 55143443 | missense variant | G/A | snv | 5.2E-05 | 2.1E-05 | 5 | |
rs121913430 | 1.000 | 0.080 | 7 | 55174740 | missense variant | G/A | snv | 3 |