Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12203592 | 0.649 | 0.320 | 6 | 396321 | intron variant | C/T | snv | 0.10 | 5 | ||
rs8070723 | 0.851 | 0.240 | 17 | 46003698 | intron variant | A/G | snv | 0.18 | 5 | ||
rs6687758 | 0.763 | 0.200 | 1 | 221991606 | regulatory region variant | A/G | snv | 0.20 | 2 | ||
rs3849942 | 0.776 | 0.200 | 9 | 27543283 | non coding transcript exon variant | T/A;C | snv | 2 | |||
rs7224296 | 0.882 | 0.160 | 17 | 46722680 | intron variant | G/A | snv | 0.59 | 2 | ||
rs2142991 | 1.000 | 0.120 | 10 | 42845657 | intergenic variant | C/G;T | snv | 1 | |||
rs6852535 | 1.000 | 0.120 | 4 | 122557561 | intergenic variant | G/A | snv | 0.24 | 1 | ||
rs7571971 | 1.000 | 0.120 | 2 | 88595833 | non coding transcript exon variant | T/C | snv | 0.70 | 0.77 | 1 | |
rs6547705 | 1.000 | 0.120 | 2 | 86817193 | intron variant | G/A | snv | 0.83 | 1 | ||
rs75932628 | 0.662 | 0.480 | 6 | 41161514 | missense variant | C/A;T | snv | 6.8E-05; 2.6E-03 | 1 | ||
rs242557 | 0.752 | 0.200 | 17 | 45942346 | intron variant | G/A | snv | 0.36 | 1 | ||
rs1768208 | 0.851 | 0.200 | 3 | 39481512 | intron variant | T/C | snv | 0.76 | 1 | ||
rs11568563 | 0.925 | 0.240 | 12 | 21304500 | missense variant | T/G | snv | 4.5E-02 | 4.4E-02 | 1 | |
rs1411478 | 0.925 | 0.120 | 1 | 180993146 | intron variant | A/G | snv | 0.56 | 1 |