Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137929307 | 0.752 | 0.240 | 19 | 11116928 | missense variant | G/A | snv | 4.4E-05 | 4.9E-05 | 10 | |
rs139043155 | 0.790 | 0.200 | 19 | 11106668 | missense variant | T/A | snv | 3.2E-05 | 4.2E-05 | 10 | |
rs28942084 | 0.763 | 0.200 | 19 | 11120436 | missense variant | C/A;T | snv | 2.8E-05 | 4.2E-05 | 9 | |
rs750518671 | 0.790 | 0.200 | 19 | 11128085 | missense variant | G/A;C;T | snv | 8.0E-06 | 9 | ||
rs28942080 | 0.807 | 0.200 | 19 | 11113743 | missense variant | G/A;C;T | snv | 1.2E-05; 4.0E-06 | 8 | ||
rs373822756 | 0.807 | 0.200 | 19 | 11105568 | missense variant | A/G;T | snv | 5.2E-05 | 8 | ||
rs570942190 | 0.827 | 0.200 | 19 | 11113337 | missense variant | C/T | snv | 2.4E-05 | 7.0E-06 | 7 | |
rs879254965 | 0.827 | 0.200 | 19 | 11116140 | missense variant | G/A;C;T | snv | 7 | |||
rs121908026 | 0.851 | 0.160 | 19 | 11105436 | missense variant | C/T | snv | 1.6E-05 | 3.5E-05 | 6 | |
rs121908031 | 0.851 | 0.160 | 19 | 11120425 | stop gained | C/A;G | snv | 8.0E-06 | 6 | ||
rs267607213 | 0.851 | 0.160 | 19 | 11100286 | stop gained | G/A;T | snv | 6 | |||
rs879255038 | 0.851 | 0.160 | 19 | 11116982 | missense variant | C/G;T | snv | 4.0E-06 | 6 | ||
rs121908027 | 0.882 | 0.160 | 19 | 11105557 | inframe deletion | TGG/- | delins | 5 | |||
rs121908035 | 0.882 | 0.160 | 19 | 11105599 | stop gained | C/A;G | snv | 5 | |||
rs373646964 | 0.882 | 0.160 | 19 | 11113650 | missense variant | G/A;C | snv | 2.4E-05; 4.0E-06 | 5 | ||
rs730882090 | 0.882 | 0.160 | 19 | 11107420 | missense variant | C/A | snv | 4.0E-06 | 7.0E-06 | 5 | |
rs879254405 | 0.882 | 0.160 | 19 | 11100255 | missense variant | T/G | snv | 5 | |||
rs879254600 | 0.882 | 0.160 | 19 | 11105532 | missense variant | G/A | snv | 5 | |||
rs879255130 | 0.882 | 0.160 | 19 | 11120446 | frameshift variant | C/-;CC | delins | 5 |