Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs587782664 | 0.742 | 0.320 | 17 | 7674252 | missense variant | C/A;G;T | snv | 4.0E-06 | 14 | ||
rs765848205 | 0.763 | 0.240 | 17 | 7674253 | missense variant | A/C;G;T | snv | 12 | |||
rs121913287 | 0.752 | 0.400 | 3 | 179199088 | missense variant | G/A | snv | 11 | |||
rs867262025 | 0.790 | 0.360 | 3 | 179221146 | missense variant | G/A | snv | 9 | |||
rs1057519928 | 0.807 | 0.200 | 3 | 179221147 | missense variant | A/C | snv | 8 | |||
rs779707422 | 0.763 | 0.280 | 8 | 38417331 | missense variant | G/A;T | snv | 4.0E-06 | 7 | ||
rs1057519898 | 0.851 | 0.120 | 8 | 38417333 | missense variant | T/C | snv | 5 | |||
rs1057519899 | 0.851 | 0.120 | 8 | 38417879 | missense variant | T/C | snv | 5 | |||
rs1057519906 | 0.882 | 0.120 | 15 | 90088607 | missense variant | T/A;C | snv | 5 | |||
rs121913503 | 0.689 | 0.200 | 15 | 90088606 | missense variant | C/A;T | snv | 5 | |||
rs1057519902 | 0.742 | 0.160 | 1 | 226064451 | missense variant | G/C | snv | 4 | |||
rs1057519888 | 0.925 | 0.080 | 7 | 55143386 | missense variant | A/G | snv | 3 | |||
rs139236063 | 0.925 | 0.080 | 7 | 55165350 | missense variant | G/C;T | snv | 3 | |||
rs387906589 | 0.925 | 0.120 | 2 | 157766004 | missense variant | C/A;T | snv | 3 | |||
rs863224846 | 0.882 | 0.160 | 2 | 157770386 | missense variant | T/C;G | snv | 4.0E-06 | 3 | ||
rs1057519875 | 0.925 | 0.120 | 2 | 157770385 | missense variant | C/A | snv | 2 | |||
rs1057519903 | 0.683 | 0.080 | 1 | 226064434 | missense variant | A/T | snv | 2 | |||
rs1057519904 | 0.742 | 0.080 | 6 | 27872233 | missense variant | T/A | snv | 2 | |||
rs1057519905 | 0.925 | 0.080 | 6 | 27872234 | missense variant | T/C | snv | 2 | |||
rs148924904 | 0.724 | 0.360 | 17 | 7675124 | missense variant | T/C | snv | 7.0E-06 | 17 |