Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121908670 | 0.882 | 0.080 | 11 | 68363784 | missense variant | G/A | 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 | 2 | ||
rs1320065036 | 0.925 | 0.160 | 11 | 68386342 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 2 | |
rs866606166 | 1.000 | 0.120 | 11 | 68386678 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs201320326 | 1.000 | 0.120 | 11 | 68386499 | missense variant | C/A;T | snv | 2.2E-04 | 1 | ||
rs121908665 | 1.000 | 0.120 | 11 | 68403606 | missense variant | C/T | snv | 1 | |||
rs121908664 | 1.000 | 0.120 | 11 | 68389949 | missense variant | G/A | snv | 1 | |||
rs1318906451 | 1.000 | 0.120 | 11 | 68389900 | missense variant | T/A | snv | 4.0E-06 | 1 | ||
rs397514665 | 1.000 | 0.120 | 11 | 68363791 | missense variant | C/T | snv | 1.2E-05 | 1 | ||
rs377258285 | 1.000 | 0.120 | 11 | 68425202 | missense variant | C/T | snv | 5.6E-05 | 6.3E-05 | 1 | |
rs746701187 | 1.000 | 0.120 | 11 | 68410019 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs545508982 | 1.000 | 0.120 | 11 | 68389980 | stop gained | G/A;T | snv | 4.0E-06; 8.0E-06 | 1 | ||
rs757888034 | 1.000 | 0.120 | 11 | 68386600 | missense variant | G/A;T | snv | 1.2E-05; 4.0E-06 | 1.4E-05 | 1 | |
rs750791263 | 1.000 | 0.120 | 11 | 68386510 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs760548029 | 1.000 | 0.120 | 11 | 68357768 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs1273567061 | 1.000 | 0.120 | 11 | 68386525 | missense variant | A/G | snv | 4.0E-06 | 2.1E-05 | 1 | |
rs1470530779 | 1.000 | 0.120 | 11 | 68406769 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs1219101402 | 1.000 | 0.120 | 11 | 68365607 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
rs1158745675 | 1.000 | 0.120 | 11 | 68386367 | stop gained | C/A;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
rs121908671 | 0.851 | 0.120 | 11 | 68357801 | missense variant | G/A | snv | 1 | |||
rs121908672 | 0.925 | 0.080 | 11 | 68357802 | missense variant | C/T | snv | 1 | |||
rs121908669 | 1.000 | 0.040 | 11 | 68357672 | missense variant | G/C | snv | 1 | |||
rs121908673 | 0.925 | 0.160 | 11 | 68363818 | missense variant | C/T | snv | 1 | |||
rs201030241 | 1.000 | 0.080 | 11 | 68446497 | missense variant | A/G | snv | 3.7E-04 | 5.6E-05 | 1 | |
rs1332274863 | 1.000 | 0.080 | 11 | 68386441 | missense variant | G/A | snv | 4.0E-06 | 1 |