Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 35 | ||
rs9895661 | 0.882 | 0.200 | 17 | 61379228 | non coding transcript exon variant | C/T | snv | 0.69 | 7 | ||
rs6123359 | 1.000 | 0.080 | 20 | 54098167 | regulatory region variant | A/G | snv | 0.12 | 2 | ||
rs17265703 | 3 | 122329797 | intron variant | A/G | snv | 0.12 | 2 | ||||
rs1550532 | 2 | 233356202 | intron variant | C/G | snv | 0.75 | 2 | ||||
rs34339006 | 1.000 | 0.040 | 2 | 233362876 | intron variant | C/T | snv | 0.32 | 2 | ||
rs10934582 | 3 | 122294507 | downstream gene variant | G/A | snv | 0.28 | 1 | ||||
rs11101061 | 10 | 49244632 | intergenic variant | T/A | snv | 0.10 | 1 | ||||
rs12517041 | 5 | 23301799 | downstream gene variant | A/G | snv | 0.15 | 1 | ||||
rs12901379 | 15 | 50692447 | downstream gene variant | A/C;G;T | snv | 1 | |||||
rs13068893 | 3 | 122307242 | regulatory region variant | C/G | snv | 8.7E-02 | 1 | ||||
rs13301969 | 9 | 126532675 | downstream gene variant | C/T | snv | 0.33 | 1 | ||||
rs17711722 | 7 | 65806210 | downstream gene variant | C/T | snv | 1 | |||||
rs4678181 | 3 | 122320183 | downstream gene variant | G/A | snv | 8.6E-02 | 1 | ||||
rs11967485 | 6 | 156807123 | intron variant | G/A | snv | 0.15 | 1 | ||||
rs11105380 | 12 | 89702020 | intron variant | T/A | snv | 0.24 | 1 | ||||
rs7481584 | 11 | 3007859 | non coding transcript exon variant | G/A | snv | 0.27 | 1 | ||||
rs11918240 | 3 | 122226991 | intron variant | A/G;T | snv | 1 | |||||
rs17251221 | 0.724 | 0.360 | 3 | 122274400 | intron variant | A/G | snv | 0.11 | 1 | ||
rs1801725 | 0.633 | 0.600 | 3 | 122284910 | missense variant | G/T | snv | 0.13 | 0.11 | 1 | |
rs4678176 | 3 | 122290328 | 3 prime UTR variant | A/G | snv | 9.1E-02 | 1 | ||||
rs1570669 | 0.925 | 0.080 | 20 | 54157888 | intron variant | A/G | snv | 0.42 | 1 | ||
rs13103813 | 4 | 3466709 | intron variant | A/C | snv | 0.62 | 1 | ||||
rs3109133 | 2 | 132545965 | intron variant | C/G;T | snv | 1 | |||||
rs4685771 | 3 | 4586857 | intron variant | C/T | snv | 0.20 | 1 |