Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519696 | 1.000 | 0.040 | 2 | 29214054 | missense variant | C/T | snv | 5 | |||
rs1057519793 | 0.882 | 0.040 | 5 | 177095551 | missense variant | T/A | snv | 3 | |||
rs766121173 | 0.882 | 0.040 | 5 | 177095625 | missense variant | G/A | snv | 1.1E-04 | 6.3E-05 | 3 | |
rs774829510 | 0.882 | 0.040 | 9 | 21971046 | missense variant | C/A;T | snv | 3 | |||
rs1057519792 | 1.000 | 0.040 | 5 | 177095415 | missense variant | C/A;G | snv | 1 | |||
rs147055703 | 1.000 | 0.040 | X | 48698902 | missense variant | G/A | snv | 1.3E-04 | 1.9E-05 | 1 | |
rs3211371 | 0.827 | 0.080 | 19 | 41016810 | missense variant | C/A;T | snv | 1.2E-04; 8.8E-02 | 6 | ||
rs1131691021 | 0.716 | 0.120 | 17 | 7675097 | missense variant | A/C;G | snv | 21 | |||
rs1196220479 | 0.851 | 0.120 | 11 | 102223635 | missense variant | G/A | snv | 4.0E-06 | 4 | ||
rs2279343 | 0.776 | 0.200 | 19 | 41009358 | missense variant | A/G | snv | 0.13 | 8 | ||
rs80357989 | 0.882 | 0.200 | 17 | 43094680 | frameshift variant | -/TAATGAG | delins | 4 | |||
rs121918453 | 0.732 | 0.280 | 12 | 112450394 | missense variant | G/A;C;T | snv | 19 | |||
rs762846821 | 0.614 | 0.320 | 17 | 7675151 | missense variant | C/A;T | snv | 8.0E-06 | 57 | ||
rs2229080 | 0.742 | 0.320 | 18 | 52906232 | missense variant | C/A;G | snv | 0.45 | 16 | ||
rs1444669684 | 0.658 | 0.480 | 9 | 21994285 | missense variant | C/A;T | snv | 36 | |||
rs1057519975 | 0.649 | 0.480 | 17 | 7675209 | missense variant | A/C;G;T | snv | 34 | |||
rs104894228 | 0.605 | 0.560 | 11 | 534286 | missense variant | C/A;G;T | snv | 48 | |||
rs28934576 | 0.554 | 0.600 | 17 | 7673802 | missense variant | C/A;G;T | snv | 4.0E-06; 1.6E-05 | 78 | ||
rs104894229 | 0.564 | 0.600 | 11 | 534289 | missense variant | C/A;G;T | snv | 73 | |||
rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 144 |