Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs587778556 | 2 | 177231705 | missense variant | G/A | snv | 3.2E-05 | 4.9E-05 | 2 | |||
rs755135182 | 2 | 177231657 | missense variant | G/A | snv | 4.0E-06 | 2 | ||||
rs12471433 | 2 | 177257637 | intron variant | A/C | snv | 0.29 | 1 | ||||
rs17581525 | 2 | 177281634 | intron variant | C/G | snv | 0.26 | 1 | ||||
rs34468415 | 2 | 177260414 | intron variant | A/G | snv | 0.28 | 1 | ||||
rs35284526 | 2 | 177256796 | intron variant | C/A;G;T | snv | 1 | |||||
rs35955110 | 2 | 177278643 | intron variant | T/C | snv | 0.29 | 1 | ||||
rs6433657 | 2 | 177269949 | intron variant | A/G;T | snv | 1 | |||||
rs6721961 | 0.672 | 0.520 | 2 | 177265309 | intron variant | T/C;G | snv | 0.89 | 24 | ||
rs1057519921 | 0.763 | 0.240 | 2 | 177234231 | missense variant | T/C | snv | 10 | |||
rs35652124 | 0.790 | 0.320 | 2 | 177265345 | intron variant | T/C | snv | 0.29 | 8 | ||
rs1057519920 | 0.790 | 0.160 | 2 | 177234232 | missense variant | C/A;G;T | snv | 7 | |||
rs1057519922 | 0.790 | 0.200 | 2 | 177234082 | missense variant | C/G;T | snv | 7 | |||
rs1057519923 | 0.807 | 0.200 | 2 | 177234081 | missense variant | T/A | snv | 6 | |||
rs1057519924 | 0.807 | 0.200 | 2 | 177234080 | missense variant | C/A | snv | 6 | |||
rs6726395 | 0.851 | 0.240 | 2 | 177238501 | intron variant | A/G | snv | 0.52 | 4 | ||
rs750553272 | 0.851 | 0.080 | 2 | 177230898 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 4 | |
rs746497256 | 0.925 | 0.080 | 2 | 177231925 | synonymous variant | A/G | snv | 8.0E-06 | 7.0E-06 | 3 | |
rs1553488015 | 0.925 | 0.080 | 2 | 177234226 | missense variant | C/T | snv | 2 | |||
rs767964519 | 0.925 | 0.120 | 2 | 177231869 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs10497511 | 1.000 | 0.080 | 2 | 177254568 | intron variant | G/A;C | snv | 1 | |||
rs1185894299 | 1.000 | 0.040 | 2 | 177232545 | synonymous variant | A/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs1434704960 | 1.000 | 0.080 | 2 | 177231543 | missense variant | C/T | snv | 1 | |||
rs1469602964 | 1.000 | 0.040 | 2 | 177233301 | missense variant | A/T | snv | 4.1E-06 | 1 | ||
rs1553487942 | 1.000 | 2 | 177234076 | missense variant | C/T | snv | 1 |