Source: CURATED
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs377325220 | 1.000 | 0.120 | 1 | 155238621 | missense variant | T/C | snv | 8.0E-06 | 1 | ||
rs381427 | 1.000 | 0.120 | 1 | 155238206 | missense variant | A/C;T | snv | 1.2E-05 | 1 | ||
rs397518433 | 1.000 | 0.120 | 1 | 155240672 | frameshift variant | G/- | delins | 1 | |||
rs398123526 | 0.925 | 0.120 | 1 | 155236409 | missense variant | C/G;T | snv | 1.2E-05; 4.0E-06 | 1 | ||
rs398123528 | 1.000 | 0.120 | 1 | 155235829 | missense variant | C/A;G | snv | 4.0E-06 | 1 | ||
rs74462743 | 0.925 | 0.120 | 1 | 155238194 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
rs74598136 | 0.925 | 0.120 | 1 | 155235750 | missense variant | G/A | snv | 1 | |||
rs74731340 | 1.000 | 0.120 | 1 | 155237411 | missense variant | C/T | snv | 1 | |||
rs74752878 | 1.000 | 0.120 | 1 | 155235699 | missense variant | T/C | snv | 1 | |||
rs749416070 | 1.000 | 0.120 | 1 | 155238269 | missense variant | C/G;T | snv | 4.3E-05 | 1 | ||
rs74979486 | 1.000 | 0.120 | 1 | 155236276 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
rs75243000 | 1.000 | 0.120 | 1 | 155235762 | missense variant | A/G | snv | 1 | |||
rs75385858 | 1.000 | 0.120 | 1 | 155235765 | missense variant | T/G | snv | 1 | |||
rs75528494 | 1.000 | 0.120 | 1 | 155236254 | missense variant | G/C;T | snv | 1 | |||
rs75548401 | 0.882 | 0.160 | 1 | 155236246 | missense variant | G/A | snv | 5.9E-03 | 6.2E-03 | 1 | |
rs75564605 | 1.000 | 0.120 | 1 | 155235747 | missense variant | A/G | snv | 1 | |||
rs757041827 | 1.000 | 0.120 | 1 | 155240641 | missense variant | G/A;C | snv | 2.0E-05; 8.0E-06 | 1 | ||
rs76026102 | 1.000 | 0.120 | 1 | 155238164 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs76071730 | 1.000 | 0.120 | 1 | 155235231 | missense variant | T/C;G | snv | 1.2E-05 | 1 | ||
rs76228122 | 1.000 | 0.120 | 1 | 155236264 | missense variant | T/C | snv | 1 | |||
rs76500263 | 1.000 | 0.120 | 1 | 155238293 | missense variant | T/G | snv | 1 | |||
rs765633380 | 1.000 | 0.120 | 1 | 155237370 | missense variant | G/A | snv | 2.0E-05 | 7.0E-06 | 1 | |
rs76725886 | 0.925 | 0.120 | 1 | 155237531 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
rs76910485 | 1.000 | 0.120 | 1 | 155235780 | missense variant | G/A | snv | 1 | |||
rs772548282 | 1.000 | 0.120 | 1 | 155235798 | missense variant | A/G | snv | 1 |