Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121908245 | 1.000 | 0.080 | 19 | 13332911 | missense variant | C/T | snv | 8.1E-06 | 7.0E-06 | 1 | |
rs121908212 | 0.732 | 0.160 | 19 | 13303877 | missense variant | G/A | snv | 14 | |||
rs1057520918 | 0.790 | 0.160 | 19 | 13262780 | missense variant | C/T | snv | 11 | |||
rs121908217 | 0.851 | 0.120 | 19 | 13308452 | missense variant | C/T | snv | 4.0E-06 | 9 | ||
rs886037945 | 0.827 | 0.160 | 19 | 13303584 | missense variant | C/T | snv | 6 | |||
rs121908247 | 0.851 | 0.160 | 19 | 13235693 | missense variant | C/T | snv | 5 | |||
rs794727411 | 0.851 | 0.160 | 19 | 13261526 | missense variant | C/G;T | snv | 5 | |||
rs121909324 | 0.851 | 0.160 | 19 | 13255217 | stop gained | G/A | snv | 4 | |||
rs121908215 | 0.882 | 0.160 | 19 | 13359707 | missense variant | C/T | snv | 3 | |||
rs121909326 | 0.882 | 0.160 | 19 | 13235219 | missense variant | A/G | snv | 3 | |||
rs863224852 | 0.882 | 0.160 | 19 | 13359680 | missense variant | C/T | snv | 3 |