Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9904341 | 0.695 | 0.280 | 17 | 78214286 | 5 prime UTR variant | G/A;C;T | snv | 0.38; 4.8E-06 | 20 | ||
rs989692988 | 17 | 7676023 | splice donor variant | A/C | snv | 8.0E-06 | 1 | ||||
rs9869263 | 0.925 | 0.080 | 3 | 190312891 | synonymous variant | A/C;G;T | snv | 8.0E-06; 0.83; 4.0E-06 | 3 | ||
rs9862 | 1.000 | 0.080 | 22 | 32857293 | missense variant | T/A;C | snv | 4.0E-06; 0.55 | 3 | ||
rs9856 | 0.925 | 0.120 | X | 123911791 | 3 prime UTR variant | C/T | snv | 0.57 | 4 | ||
rs9836340 | 3 | 89356604 | intron variant | A/G | snv | 0.33 | 1 | ||||
rs976306779 | 0.851 | 0.080 | X | 67545492 | missense variant | C/A;T | snv | 6.6E-06 | 8 | ||
rs975580838 | 3 | 189868592 | synonymous variant | G/A | snv | 1 | |||||
rs975052107 | 3 | 52563348 | missense variant | A/G | snv | 1 | |||||
rs975030738 | 11 | 2135469 | missense variant | C/T | snv | 1 | |||||
rs974296289 | 12 | 106247384 | synonymous variant | C/T | snv | 1 | |||||
rs971586985 | 1.000 | 0.160 | 1 | 193212458 | missense variant | G/A;T | snv | 4.0E-06 | 2.1E-05 | 2 | |
rs969139366 | 4 | 54277974 | missense variant | T/C | snv | 3.5E-05 | 3 | ||||
rs966423 | 0.776 | 0.200 | 2 | 217445617 | intron variant | C/G;T | snv | 11 | |||
rs965513 | 0.742 | 0.200 | 9 | 97793827 | intron variant | A/G;T | snv | 12 | |||
rs9642880 | 0.776 | 0.240 | 8 | 127705823 | intron variant | G/A;T | snv | 8 | |||
rs9600079 | 0.925 | 0.080 | 13 | 73154002 | intergenic variant | G/T | snv | 0.46 | 5 | ||
rs959969530 | 17 | 39727763 | missense variant | G/A | snv | 1 | |||||
rs9589207 | 0.925 | 0.080 | 13 | 91351335 | mature miRNA variant | G/A;C | snv | 5.4E-03; 4.0E-06 | 4 | ||
rs9568036 | 1.000 | 0.080 | 13 | 48397800 | intron variant | G/A;T | snv | 2 | |||
rs9533156 | 0.807 | 0.280 | 13 | 42573535 | intron variant | T/C | snv | 0.47 | 7 | ||
rs9513008 | 13 | 28053535 | intron variant | C/T | snv | 1 | |||||
rs9503518 | 6 | 3273223 | synonymous variant | A/G | snv | 8.6E-02 | 9.0E-02 | 1 | |||
rs944289 | 0.742 | 0.200 | 14 | 36180040 | upstream gene variant | C/T | snv | 0.45 | 15 | ||
rs942190 | 1.000 | 0.080 | 14 | 89956320 | intron variant | T/C | snv | 0.37 | 2 |