Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1333048 | 0.683 | 0.320 | 9 | 22125348 | intron variant | A/C | snv | 0.44 | 7 | ||
rs11216126 | 1.000 | 0.040 | 11 | 116746524 | downstream gene variant | A/C | snv | 0.11 | 3 | ||
rs12988520 | 1.000 | 0.040 | 2 | 233698748 | intron variant | A/C | snv | 0.51 | 2 | ||
rs1797912 | 1.000 | 0.040 | 3 | 12428740 | intron variant | A/C | snv | 0.33 | 2 | ||
rs295 | 1.000 | 0.040 | 8 | 19958727 | intron variant | A/C | snv | 0.28 | 1 | ||
rs8179252 | 0.882 | 0.120 | 2 | 27523965 | downstream gene variant | A/C | snv | 0.37 | 1 | ||
rs2943634 | 0.763 | 0.200 | 2 | 226203364 | intergenic variant | A/C;G | snv | 5 | |||
rs6589567 | 1.000 | 0.040 | 11 | 116799960 | intergenic variant | A/C;G;T | snv | 3 | |||
rs1441756 | 1.000 | 0.040 | 8 | 20010875 | intergenic variant | A/C;G;T | snv | 1 | |||
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 7 | ||
rs180349 | 0.925 | 0.200 | 11 | 116741111 | intergenic variant | A/C;T | snv | 3 | |||
rs7041 | 0.576 | 0.800 | 4 | 71752617 | missense variant | A/C;T | snv | 0.52; 4.0E-06 | 3 | ||
rs8192284 | 0.724 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 3 | |||
rs13022873 | 0.882 | 0.120 | 2 | 27592643 | intron variant | A/C;T | snv | 2 | |||
rs2237895 | 0.790 | 0.240 | 11 | 2835964 | intron variant | A/C;T | snv | 1 | |||
rs486394 | 1.000 | 0.040 | 11 | 116655605 | intron variant | A/C;T | snv | 1 | |||
rs1535 | 0.752 | 0.240 | 11 | 61830500 | intron variant | A/G | snv | 0.31 | 18 | ||
rs10938397 | 0.851 | 0.200 | 4 | 45180510 | intergenic variant | A/G | snv | 0.37 | 8 | ||
rs9987289 | 1.000 | 0.040 | 8 | 9325848 | non coding transcript exon variant | A/G | snv | 0.87 | 8 | ||
rs929596 | 0.925 | 0.040 | 2 | 233765830 | intron variant | A/G | snv | 0.32 | 7 | ||
rs11708067 | 0.882 | 0.080 | 3 | 123346931 | intron variant | A/G | snv | 0.19 | 5 | ||
rs1800625 | 0.641 | 0.680 | 6 | 32184665 | upstream gene variant | A/G | snv | 0.15 | 4 | ||
rs780092 | 0.827 | 0.160 | 2 | 27520287 | intron variant | A/G | snv | 0.18 | 4 | ||
rs1919128 | 0.882 | 0.120 | 2 | 27578892 | missense variant | A/G | snv | 0.30 | 0.24 | 3 | |
rs2070959 | 0.742 | 0.320 | 2 | 233693545 | missense variant | A/G | snv | 0.31 | 0.30 | 3 |