Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1801725 | 0.633 | 0.600 | 3 | 122284910 | missense variant | G/T | snv | 0.13 | 0.11 | 39 | |
rs104893689 | 0.790 | 0.200 | 3 | 122261589 | missense variant | G/A;C | snv | 10 | |||
rs121909262 | 0.851 | 0.120 | 3 | 122254304 | missense variant | C/G;T | snv | 5 | |||
rs193922442 | 0.827 | 0.120 | 3 | 122261589 | frameshift variant | G/- | del | 5 | |||
rs28936684 | 0.827 | 0.160 | 3 | 122261715 | missense variant | G/A;T | snv | 4.0E-06 | 5 | ||
rs104893705 | 0.882 | 0.120 | 3 | 122283896 | stop gained | C/A;G;T | snv | 4.0E-06 | 3 | ||
rs121909259 | 0.882 | 0.160 | 3 | 122261924 | missense variant | G/A | snv | 3 | |||
rs201858689 | 0.882 | 0.120 | 3 | 122284257 | missense variant | G/T | snv | 2.8E-05 | 3 | ||
rs104893690 | 0.925 | 0.120 | 3 | 122283699 | missense variant | G/A;T | snv | 2 | |||
rs104893700 | 1.000 | 0.080 | 3 | 122283963 | missense variant | G/A | snv | 1 | |||
rs104893707 | 1.000 | 0.080 | 3 | 122261588 | stop gained | C/A;T | snv | 1.6E-05 | 1 | ||
rs104893709 | 1.000 | 0.080 | 3 | 122257175 | stop gained | G/T | snv | 1 | |||
rs1060502861 | 1.000 | 0.080 | 3 | 122282156 | missense variant | G/A | snv | 1 | |||
rs869320729 | 1.000 | 0.080 | 3 | 122284195 | frameshift variant | CC/T | delins | 1 |