Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1276519904 | 0.645 | 0.520 | 1 | 226071445 | missense variant | A/G | snv | 63 | |||
rs1557644984 | 0.925 | 0.080 | 1 | 42927622 | missense variant | A/G | snv | 5 | |||
rs587776935 | 0.827 | 0.120 | 1 | 243505296 | missense variant | G/A | snv | 7 | |||
rs587779766 | 0.851 | 0.200 | 1 | 27549742 | frameshift variant | CA/- | delins | 7 | |||
rs587779767 | 0.851 | 0.200 | 1 | 27549218 | frameshift variant | G/- | delins | 7 | |||
rs587779768 | 0.851 | 0.200 | 1 | 27549569 | frameshift variant | G/- | delins | 7 | |||
rs61751035 | 0.882 | 0.160 | 1 | 213242186 | missense variant | G/A | snv | 2.4E-05 | 1.4E-05 | 6 | |
rs730882203 | 0.851 | 0.080 | 1 | 46510953 | missense variant | C/T | snv | 6 | |||
rs752746786 | 0.742 | 0.560 | 1 | 1806503 | missense variant | A/C;G;T | snv | 4.0E-06 | 30 | ||
rs758432471 | 0.925 | 1 | 1806513 | missense variant | C/T | snv | 7.0E-06 | 4 | |||
rs869312821 | 0.882 | 0.120 | 1 | 1806515 | missense variant | T/C | snv | 7 | |||
rs869312822 | 0.827 | 0.200 | 1 | 1806514 | missense variant | A/C | snv | 8 | |||
rs869312823 | 0.882 | 0.080 | 1 | 1806509 | missense variant | T/C | snv | 9 | |||
rs869312824 | 0.827 | 0.200 | 1 | 1804565 | missense variant | A/G | snv | 14 | |||
rs869312825 | 0.827 | 0.120 | 1 | 1804548 | start lost | T/C | snv | 11 | |||
rs869312826 | 0.882 | 0.080 | 1 | 1787378 | missense variant | C/T | snv | 6 | |||
rs559979281 | 0.742 | 0.440 | 2 | 121530892 | non coding transcript exon variant | C/G;T | snv | 7.7E-06; 2.3E-05; 3.5E-04 | 23 | ||
rs863225422 | 0.742 | 0.440 | 2 | 121530927 | non coding transcript exon variant | G/A | snv | 4.6E-05; 7.7E-06 | 4.9E-05 | 23 | |
rs1114167292 | 0.882 | 0.080 | 3 | 197704686 | missense variant | C/T | snv | 1.4E-05 | 6 | ||
rs1114167298 | 0.882 | 0.120 | 3 | 6861849 | missense variant | T/C | snv | 7.0E-06 | 5 | ||
rs1114167300 | 0.925 | 0.040 | 3 | 7578878 | missense variant | C/T | snv | 6 | |||
rs1114167301 | 0.925 | 0.040 | 3 | 7578930 | missense variant | C/A;T | snv | 4.0E-06 | 6 | ||
rs1559759089 | 0.827 | 0.200 | 3 | 113795101 | missense variant | C/A | snv | 14 | |||
rs1560212751 | 1.000 | 3 | 51208772 | splice acceptor variant | A/G | snv | 2 | ||||
rs1560414254 | 1.000 | 3 | 51312486 | frameshift variant | ACTT/- | delins | 2 |