Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519825 | 0.882 | 0.120 | X | 101356176 | missense variant | C/G | snv | 1 | |||
rs1057519826 | 0.882 | 0.120 | X | 101356177 | missense variant | A/T | snv | 1 | |||
rs13114738 | 0.851 | 0.120 | 4 | 102363708 | intron variant | C/A;T | snv | 16 | |||
rs6214 | 0.672 | 0.400 | 12 | 102399791 | 3 prime UTR variant | C/T | snv | 0.45 | 1 | ||
rs11568818 | 0.763 | 0.280 | 11 | 102530930 | upstream gene variant | T/A;C | snv | 2 | |||
rs3740393 | 0.776 | 0.280 | 10 | 102876898 | intron variant | G/C;T | snv | 1 | |||
rs696217 | 0.662 | 0.640 | 3 | 10289773 | missense variant | G/T | snv | 8.8E-02 | 7.1E-02 | 2 | |
rs3753841 | 0.827 | 0.080 | 1 | 102914362 | missense variant | G/A | snv | 0.61 | 0.49 | 3 | |
rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 1 | |
rs121434592 | 0.595 | 0.640 | 14 | 104780214 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs314276 | 0.807 | 0.280 | 6 | 104960124 | intron variant | A/C | snv | 0.65 | 2 | ||
rs3018066 | 4 | 106368369 | intron variant | A/G;T | snv | 0.38 | 1 | ||||
rs450533 | 4 | 106909104 | intron variant | T/C | snv | 0.36 | 1 | ||||
rs1800057 | 0.776 | 0.200 | 11 | 108272729 | missense variant | C/A;G | snv | 1.7E-02 | 4 | ||
rs587776551 | 1.000 | 0.200 | 11 | 108281168 | missense variant | G/A;T | snv | 1.6E-05 | 1.4E-05 | 2 | |
rs1801516 | 0.627 | 0.400 | 11 | 108304735 | missense variant | G/A | snv | 0.11 | 0.11 | 3 | |
rs564652222 | 0.925 | 0.280 | 11 | 108325416 | missense variant | C/A;T | snv | 1.4E-05 | 3 | ||
rs769142993 | 0.851 | 0.280 | 11 | 108331498 | missense variant | G/C;T | snv | 2.4E-05 | 7.0E-06 | 2 | |
rs587779872 | 1.000 | 0.200 | 11 | 108345818 | missense variant | C/T | snv | 3.2E-05 | 1.4E-05 | 2 | |
rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 22 | ||
rs6533530 | 0.851 | 0.120 | 4 | 110810780 | intergenic variant | T/C | snv | 0.47 | 16 | ||
rs1805076 | 0.851 | 0.120 | 11 | 111764842 | missense variant | C/T | snv | 6.5E-03 | 7.0E-03 | 2 | |
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 29 | |
rs104894309 | 0.851 | 0.200 | 11 | 112086940 | stop gained | C/A;T | snv | 4.0E-06 | 4 | ||
rs80338845 | 0.807 | 0.240 | 11 | 112088971 | missense variant | G/T | snv | 7.0E-06 | 6 |