Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs730880140 | 1.000 | 0.080 | 11 | 47333297 | missense variant | T/C | snv | 7.0E-06 | 2 | ||
rs121913642 | 0.925 | 0.080 | 14 | 23427879 | missense variant | A/G | snv | 3 | |||
rs121913647 | 0.925 | 0.160 | 14 | 23417173 | missense variant | C/A;G;T | snv | 1.6E-05 | 3 | ||
rs397516142 | 1.000 | 0.080 | 14 | 23425357 | missense variant | C/A;G;T | snv | 8.0E-06; 1.6E-05 | 3 | ||
rs45544633 | 1.000 | 0.080 | 14 | 23417174 | missense variant | G/A | snv | 3 | |||
rs143139258 | 0.882 | 0.080 | 12 | 110913097 | missense variant | T/G | snv | 2.0E-04 | 2.9E-04 | 4 | |
rs199476317 | 0.827 | 0.080 | 15 | 63062263 | missense variant | G/A | snv | 4 | |||
rs267607490 | 0.925 | 0.160 | 2 | 219425734 | missense variant | C/T | snv | 4 | |||
rs267607581 | 0.925 | 0.080 | 1 | 156137651 | splice region variant | C/G | snv | 4 | |||
rs397516089 | 0.827 | 0.080 | 14 | 23429807 | missense variant | C/G;T | snv | 4 | |||
rs397516165 | 0.925 | 0.080 | 14 | 23424118 | missense variant | C/G;T | snv | 4 | |||
rs397516373 | 0.925 | 0.080 | 15 | 63059663 | missense variant | G/A | snv | 4 | |||
rs397516248 | 0.851 | 0.200 | 14 | 23415153 | missense variant | C/T | snv | 5 | |||
rs727503204 | 0.882 | 0.080 | 11 | 47343020 | splice donor variant | C/G;T | snv | 5 |