Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1554389088 | 0.807 | 0.160 | 7 | 44243526 | missense variant | G/A | snv | 27 | |||
rs926027867 | 0.882 | 0.040 | 5 | 150251808 | missense variant | G/A;T | snv | 12 | |||
rs1554386687 | 0.882 | 0.040 | 7 | 44242328 | missense variant | C/T | snv | 12 | |||
rs1287121256 | 0.882 | 0.040 | 5 | 150256777 | missense variant | C/G;T | snv | 7.0E-06 | 9 | ||
rs1554122526 | 0.882 | 0.040 | 5 | 150256811 | missense variant | A/G | snv | 9 | |||
rs35993949 | 0.882 | 0.040 | 8 | 67506804 | missense variant | G/C | snv | 1.5E-03 | 1.2E-03 | 9 | |
rs61738009 | 0.827 | 0.080 | 8 | 67483807 | stop gained | C/A;T | snv | 4.0E-06; 2.0E-03 | 2.5E-03 | 9 | |
rs1554402092 | 1.000 | 7 | 44254555 | missense variant | C/T | snv | 8 | ||||
rs1554121875 | 0.882 | 0.040 | 5 | 150250281 | missense variant | T/C | snv | 7 | |||
rs1554123982 | 0.925 | 0.040 | 5 | 150273157 | splice acceptor variant | C/- | delins | 7 | |||
rs113331868 | 5 | 150228191 | splice donor variant | C/A;T | snv | 6 | |||||
rs1554122129 | 0.882 | 0.040 | 5 | 150252032 | missense variant | T/A | snv | 6 | |||
rs1554122123 | 0.925 | 0.040 | 5 | 150251979 | splice donor variant | -/A | delins | 5 |