Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1027009063 | 0.925 | 0.040 | 2 | 8802974 | stop gained | G/A | snv | 2 | |||
rs10404453 | 1.000 | 0.040 | 19 | 51693235 | non coding transcript exon variant | G/A;C | snv | 2.6E-03; 5.5E-06 | 1 | ||
rs1041163 | 0.882 | 0.160 | 1 | 100718269 | upstream gene variant | T/C | snv | 0.18 | 3 | ||
rs1050501 | 0.732 | 0.440 | 1 | 161674008 | missense variant | T/C | snv | 0.16 | 0.19 | 15 | |
rs1058885 | 0.925 | 0.080 | 1 | 109923844 | missense variant | T/C | snv | 0.38 | 0.39 | 2 | |
rs11112872 | 1.000 | 0.040 | 12 | 106111556 | intron variant | T/G | snv | 0.28 | 1 | ||
rs11225395 | 0.776 | 0.360 | 11 | 102725749 | intron variant | A/C;G | snv | 11 | |||
rs113420705 | 0.925 | 0.160 | 4 | 184649399 | 5 prime UTR variant | T/C | snv | 0.31 | 4 | ||
rs11362 | 0.742 | 0.360 | 8 | 6877877 | 5 prime UTR variant | C/T | snv | 0.43 | 0.40 | 13 | |
rs1143627 | 0.605 | 0.760 | 2 | 112836810 | 5 prime UTR variant | G/A | snv | 0.56 | 47 | ||
rs1143634 | 0.597 | 0.680 | 2 | 112832813 | synonymous variant | G/A | snv | 0.19 | 0.19 | 52 | |
rs11614913 | 0.512 | 0.760 | 12 | 53991815 | mature miRNA variant | C/T | snv | 0.39 | 0.34 | 111 | |
rs1171989978 | 1.000 | 0.040 | 1 | 202159420 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs11747270 | 0.790 | 0.240 | 5 | 150879305 | intron variant | A/G | snv | 0.21 | 7 | ||
rs12449783 | 1.000 | 0.040 | 17 | 30200635 | intron variant | A/C;T | snv | 1 | |||
rs12976445 | 0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 | 20 | ||
rs12979860 | 0.547 | 0.520 | 19 | 39248147 | intron variant | C/T | snv | 0.39 | 84 | ||
rs1333048 | 0.683 | 0.320 | 9 | 22125348 | intron variant | A/C | snv | 0.44 | 24 | ||
rs1342913 | 0.851 | 0.040 | 1 | 190151895 | intron variant | G/A | snv | 0.61 | 4 | ||
rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
rs148704956 | 0.716 | 0.360 | 6 | 52187772 | missense variant | A/G | snv | 8.0E-06 | 7.0E-06 | 19 | |
rs1595009 | 1.000 | 0.040 | 4 | 73968939 | intergenic variant | C/T | snv | 0.61 | 1 | ||
rs16944 | 0.531 | 0.920 | 2 | 112837290 | upstream gene variant | A/G | snv | 0.57 | 92 | ||
rs1799750 | 0.592 | 0.760 | 11 | 102799765 | intron variant | C/- | delins | 0.50 | 48 | ||
rs1799964 | 0.608 | 0.760 | 6 | 31574531 | upstream gene variant | T/C | snv | 0.19 | 47 |