Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs442309 | 1.000 | 0.120 | 10 | 62730735 | intron variant | C/T | snv | 0.51 | 1 | ||
rs117633859 | 1.000 | 0.120 | 1 | 67162145 | intron variant | A/G | snv | 2.6E-02 | 1 | ||
rs3021304 | 1.000 | 0.120 | 6 | 32607881 | intergenic variant | G/C | snv | 0.51 | 1 | ||
rs114800139 | 1.000 | 0.120 | 6 | 32460938 | intron variant | G/A | snv | 1 | |||
rs310236 | 1.000 | 0.120 | 1 | 64868174 | non coding transcript exon variant | G/C | snv | 0.39 | 1 | ||
rs4703863 | 0.925 | 0.280 | 5 | 81980204 | intron variant | C/A;T | snv | 2 | |||
rs310241 | 0.882 | 0.360 | 1 | 64837655 | intron variant | A/G | snv | 0.37 | 3 | ||
rs4795067 | 0.882 | 0.280 | 17 | 27779649 | intron variant | A/G | snv | 0.31 | 3 | ||
rs13210247 | 0.882 | 0.280 | 6 | 111601517 | non coding transcript exon variant | A/G | snv | 0.10 | 3 | ||
rs573775 | 0.851 | 0.320 | 6 | 106316991 | intron variant | G/A | snv | 0.34 | 4 | ||
rs7356506 | 0.851 | 0.120 | 4 | 109762298 | non coding transcript exon variant | G/A | snv | 0.63 | 4 | ||
rs12569232 | 0.882 | 0.280 | 1 | 211379722 | intron variant | G/C;T | snv | 4 | |||
rs10863888 | 0.851 | 0.280 | 1 | 211329427 | intron variant | A/C;G;T | snv | 4 | |||
rs6498169 | 0.807 | 0.280 | 16 | 11155472 | non coding transcript exon variant | G/A | snv | 0.66 | 6 | ||
rs2096525 | 0.827 | 0.280 | 22 | 23894632 | non coding transcript exon variant | T/C | snv | 0.20 | 0.20 | 6 | |
rs1048709 | 0.776 | 0.320 | 6 | 31947158 | synonymous variant | A/G | snv | 0.82 | 0.85 | 8 | |
rs1800779 | 0.763 | 0.320 | 7 | 150992855 | intron variant | G/A;C | snv | 9 | |||
rs1343151 | 0.752 | 0.400 | 1 | 67253446 | intron variant | G/A | snv | 0.41 | 10 | ||
rs2488457 | 0.763 | 0.480 | 1 | 113872746 | intron variant | G/A;C | snv | 11 | |||
rs2301436 | 0.752 | 0.320 | 6 | 167024500 | intron variant | C/T | snv | 0.42 | 11 | ||
rs1884444 | 0.637 | 0.600 | 1 | 67168129 | missense variant | G/T | snv | 0.52 | 0.51 | 34 | |
rs755622 | 0.611 | 0.720 | 22 | 23894205 | intron variant | G/C | snv | 0.26 | 44 | ||
rs1883832 | 0.581 | 0.680 | 20 | 46118343 | 5 prime UTR variant | T/C | snv | 0.75 | 0.80 | 52 | |
rs7574865 | 0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 | 59 | ||
rs763780 | 0.531 | 0.720 | 6 | 52236941 | missense variant | T/C | snv | 6.7E-02 | 6.6E-02 | 87 |