Source: BEFREE
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267607906 | 1.000 | 0.160 | 3 | 37050576 | stop gained | A/C;G;T | snv | 1 | |||
rs35045067 | 0.925 | 0.160 | 3 | 37048557 | missense variant | A/C;G | snv | 4.4E-05 | 1 | ||
rs41295282 | 1.000 | 0.160 | 3 | 37001024 | missense variant | A/G | snv | 1.6E-05 | 7.0E-05 | 1 | |
rs41295284 | 0.925 | 0.160 | 3 | 37047607 | missense variant | T/A | snv | 1.9E-04 | 1.5E-04 | 1 | |
rs587778964 | 0.882 | 0.160 | 3 | 37048604 | missense variant | A/C;T | snv | 1 | |||
rs63750511 | 0.925 | 0.160 | 3 | 37040252 | missense variant | A/C;T | snv | 1 | |||
rs63750710 | 0.925 | 0.160 | 3 | 37020411 | missense variant | A/C | snv | 1 | |||
rs63750781 | 0.851 | 0.160 | 3 | 37004444 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
rs63751094 | 0.925 | 0.160 | 3 | 36996624 | stop lost | A/G;T | snv | 1 | |||
rs63751428 | 0.882 | 0.160 | 3 | 36996686 | stop gained | C/A;T | snv | 1 | |||
rs63751608 | 0.925 | 0.160 | 3 | 37042321 | missense variant | T/C | snv | 1 | |||
rs63751615 | 0.851 | 0.200 | 3 | 37012098 | stop gained | C/A;T | snv | 4.0E-06 | 1 | ||
rs63751713 | 0.925 | 0.160 | 3 | 37047531 | missense variant | C/G;T | snv | 1 | |||
rs1060504000 | 0.925 | 0.160 | 3 | 37025666 | missense variant | T/C | snv | 2 | |||
rs1260021106 | 0.925 | 0.160 | 3 | 37025645 | missense variant | A/G | snv | 1.6E-05 | 2 | ||
rs1392665848 | 0.925 | 0.160 | 3 | 37025865 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
rs587778914 | 0.925 | 0.160 | 3 | 36996645 | missense variant | A/C | snv | 2 | |||
rs587778992 | 0.882 | 0.200 | 3 | 37050606 | stop gained | C/T | snv | 2 | |||
rs63749818 | 0.925 | 0.160 | 3 | 37007002 | stop gained | C/A;G;T | snv | 2 | |||
rs63749820 | 0.882 | 0.200 | 3 | 37007046 | stop gained | C/T | snv | 2 | |||
rs63749939 | 0.851 | 0.160 | 3 | 36996702 | missense variant | G/A | snv | 2 | |||
rs63750211 | 0.882 | 0.160 | 3 | 37008904 | missense variant | A/G | snv | 2 | |||
rs63750693 | 0.882 | 0.160 | 3 | 37047652 | missense variant | T/A;C | snv | 2 | |||
rs63750791 | 0.925 | 0.160 | 3 | 37025864 | synonymous variant | C/T | snv | 1.8E-04 | 2.1E-05 | 2 | |
rs786201226 | 0.925 | 0.160 | 3 | 37014450 | synonymous variant | A/G;T | snv | 4.0E-06 | 2 |