Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs121913499 | 0.605 | 0.520 | 2 | 208248389 | missense variant | G/A;C;T | snv | 51 | |||
rs78311289 | 0.689 | 0.440 | 4 | 1806162 | missense variant | A/C;G | snv | 4.0E-06 | 25 | ||
rs4730222 | 0.851 | 0.040 | 7 | 107169848 | 5 prime UTR variant | G/A;C;T | snv | 4 | |||
rs1035549573 | 0.882 | 0.120 | 21 | 36767227 | missense variant | C/T | snv | 8.0E-06 | 3 | ||
rs587776540 | 1.000 | 0.040 | 8 | 118110512 | frameshift variant | CACTTTGG/- | delins | 1 | |||
rs773198507 | 1.000 | 0.040 | 8 | 118110148 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs76901081 | 1.000 | 0.040 | 11 | 44124941 | missense variant | G/A | snv | 5.7E-04 | 2.0E-04 | 1 |