Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5882115 | 1.000 | 0.120 | 7 | 7233965 | intron variant | -/C | delins | 7.6E-02 | 1 | ||
rs1799752 | 0.677 | 0.480 | 17 | 63488529 | intron variant | -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT | delins | 25 | |||
rs5186 | 0.630 | 0.560 | 3 | 148742201 | 3 prime UTR variant | A/C | snv | 0.23 | 0.21 | 38 | |
rs4646 | 0.716 | 0.360 | 15 | 51210647 | 3 prime UTR variant | A/C | snv | 0.67 | 0.70 | 16 | |
rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 113 | ||
rs2228570 | 0.521 | 0.760 | 12 | 47879112 | start lost | A/C;G;T | snv | 0.63 | 99 | ||
rs9138 | 0.776 | 0.360 | 4 | 87983190 | 3 prime UTR variant | A/C;T | snv | 12 | |||
rs1805087 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 135 | |
rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 134 | |
rs4880 | 0.500 | 0.840 | 6 | 159692840 | missense variant | A/G | snv | 0.48 | 0.47 | 131 | |
rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 108 | ||
rs16944 | 0.531 | 0.920 | 2 | 112837290 | upstream gene variant | A/G | snv | 0.57 | 92 | ||
rs3077 | 0.701 | 0.440 | 6 | 33065245 | 3 prime UTR variant | A/G | snv | 0.29 | 16 | ||
rs9277535 | 0.724 | 0.440 | 6 | 33087084 | 3 prime UTR variant | A/G | snv | 0.25 | 13 | ||
rs660895 | 0.752 | 0.360 | 6 | 32609603 | intergenic variant | A/G | snv | 0.19 | 10 | ||
rs3803800 | 0.807 | 0.240 | 17 | 7559652 | missense variant | A/G | snv | 0.70 | 0.64 | 7 | |
rs3218977 | 0.807 | 0.240 | 2 | 102024739 | 3 prime UTR variant | A/G | snv | 0.14 | 6 | ||
rs859 | 0.807 | 0.200 | 15 | 81308981 | 3 prime UTR variant | A/G | snv | 0.33 | 6 | ||
rs9275224 | 0.851 | 0.200 | 6 | 32692101 | TF binding site variant | A/G | snv | 0.53 | 5 | ||
rs2856717 | 1.000 | 0.120 | 6 | 32702531 | downstream gene variant | A/G | snv | 0.64 | 2 | ||
rs17019602 | 1.000 | 0.120 | 1 | 107646236 | intron variant | A/G | snv | 0.19 | 1 | ||
rs2072392 | 1.000 | 0.120 | 22 | 17743846 | synonymous variant | A/G | snv | 2.8E-02 | 4.1E-02 | 1 | |
rs2738048 | 1.000 | 0.120 | 8 | 6965263 | downstream gene variant | A/G | snv | 0.28 | 1 | ||
rs4288398 | 1.000 | 0.120 | 8 | 7024116 | downstream gene variant | A/G | snv | 0.70 | 1 | ||
rs761991666 | 1.000 | 0.120 | 7 | 7234516 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 1 |