Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121908668 | 0.882 | 0.240 | 11 | 68357673 | missense variant | G/T | snv | 5 | |||
rs121908674 | 0.882 | 0.160 | 11 | 68410076 | missense variant | C/G;T | snv | 3 | |||
rs80358305 | 0.882 | 0.160 | 11 | 68348188 | missense variant | C/T | snv | 3 | |||
rs80358313 | 0.882 | 0.160 | 11 | 68406550 | missense variant | G/A;C;T | snv | 1.2E-05; 1.2E-05; 3.2E-05 | 3 | ||
rs1320065036 | 0.925 | 0.160 | 11 | 68386342 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 2 | |
rs1057519574 | 1.000 | 0.120 | 11 | 68347960 | missense variant | G/T | snv | 1 | |||
rs1057519575 | 1.000 | 0.120 | 11 | 68446434 | splice acceptor variant | A/G | snv | 1 | |||
rs1158745675 | 1.000 | 0.120 | 11 | 68386367 | stop gained | C/A;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
rs121908660 | 1.000 | 0.120 | 11 | 68312743 | stop gained | G/A | snv | 1 | |||
rs121908661 | 1.000 | 0.120 | 11 | 68386582 | stop gained | C/T | snv | 1 | |||
rs121908662 | 1.000 | 0.120 | 11 | 68409971 | frameshift variant | -/T | delins | 1 | |||
rs121908663 | 1.000 | 0.120 | 11 | 68413742 | stop gained | C/T | snv | 1 | |||
rs121908664 | 1.000 | 0.120 | 11 | 68389949 | missense variant | G/A | snv | 1 | |||
rs121908665 | 1.000 | 0.120 | 11 | 68403606 | missense variant | C/T | snv | 1 | |||
rs121908666 | 1.000 | 0.120 | 11 | 68389921 | stop gained | G/T | snv | 1 | |||
rs121908667 | 1.000 | 0.120 | 11 | 68410024 | stop gained | G/A | snv | 7.0E-06 | 1 | ||
rs1219101402 | 1.000 | 0.120 | 11 | 68365607 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
rs1273567061 | 1.000 | 0.120 | 11 | 68386525 | missense variant | A/G | snv | 4.0E-06 | 2.1E-05 | 1 | |
rs1318906451 | 1.000 | 0.120 | 11 | 68389900 | missense variant | T/A | snv | 4.0E-06 | 1 | ||
rs1470530779 | 1.000 | 0.120 | 11 | 68406769 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs149645175 | 1.000 | 0.120 | 11 | 68448822 | stop gained | C/G;T | snv | 3.7E-05 | 1 | ||
rs1554967141 | 1.000 | 0.120 | 11 | 68389935 | frameshift variant | G/- | delins | 1 | |||
rs1554967176 | 1.000 | 0.120 | 11 | 68390053 | splice donor variant | G/A | snv | 1 | |||
rs1554971145 | 1.000 | 0.120 | 11 | 68410126 | frameshift variant | G/- | delins | 1 | |||
rs201320326 | 1.000 | 0.120 | 11 | 68386499 | missense variant | C/A;T | snv | 2.2E-04 | 1 |