Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1813443 | 1.000 | 0.040 | 11 | 100140279 | intron variant | G/A;C | snv | 1 | |||
rs1734907 | 0.925 | 0.080 | 7 | 100717894 | upstream gene variant | A/G | snv | 0.84 | 4 | ||
rs314313 | 1.000 | 0.040 | 7 | 100825743 | intron variant | T/A;C;G | snv | 0.29 | 2 | ||
rs1277073914 | 0.925 | 0.040 | 7 | 100992117 | missense variant | T/A | snv | 2 | |||
rs16910526 | 0.742 | 0.280 | 12 | 10118488 | stop gained | A/C;G | snv | 6.2E-02 | 12 | ||
rs503734 | 1.000 | 0.040 | 3 | 101304904 | intron variant | A/G | snv | 0.40 | 2 | ||
rs13107612 | 0.827 | 0.120 | 4 | 101818823 | intron variant | C/T | snv | 0.31 | 5 | ||
rs13126505 | 1.000 | 0.040 | 4 | 101944147 | intron variant | G/A | snv | 4.1E-02 | 3 | ||
rs34592089 | 1.000 | 0.040 | 4 | 102005766 | intron variant | G/A;T | snv | 2 | |||
rs4851529 | 0.827 | 0.120 | 2 | 102030838 | downstream gene variant | G/A | snv | 0.44 | 5 | ||
rs10185424 | 0.925 | 0.040 | 2 | 102046427 | intron variant | T/G | snv | 0.62 | 2 | ||
rs871656 | 0.827 | 0.120 | 2 | 102154822 | intron variant | T/A;C | snv | 5 | |||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 34 | ||
rs13001325 | 1.000 | 0.040 | 2 | 102322576 | intron variant | C/T | snv | 0.30 | 3 | ||
rs13015714 | 0.882 | 0.200 | 2 | 102355405 | intron variant | G/T | snv | 0.77 | 3 | ||
rs12987977 | 0.827 | 0.120 | 2 | 102358876 | intron variant | T/G | snv | 0.31 | 5 | ||
rs2058660 | 0.882 | 0.280 | 2 | 102437989 | intron variant | G/A | snv | 0.78 | 4 | ||
rs6708413 | 1.000 | 0.040 | 2 | 102446909 | intron variant | G/A | snv | 0.78 | 2 | ||
rs917997 | 0.701 | 0.480 | 2 | 102454108 | downstream gene variant | T/A;C | snv | 20 | |||
rs2075184 | 0.724 | 0.240 | 2 | 102464132 | intergenic variant | T/C | snv | 0.78 | 14 | ||
rs28362491 | 0.592 | 0.720 | 4 | 102500998 | non coding transcript exon variant | ATTG/- | delins | 56 | |||
rs3774937 | 0.776 | 0.280 | 4 | 102513096 | intron variant | T/C | snv | 0.26 | 9 | ||
rs230534 | 0.882 | 0.120 | 4 | 102527884 | intron variant | T/C | snv | 0.73 | 3 | ||
rs7705924 | 1.000 | 0.040 | 5 | 102611094 | intron variant | A/G | snv | 5.1E-02 | 1 | ||
rs1799969 | 0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 | 38 |