Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs746147592 | 1.000 | 0.160 | X | 100665627 | missense variant | G/A;C | snv | 5.5E-06 | 2 | ||
rs121909497 | 0.925 | 0.080 | 11 | 102955390 | missense variant | A/G | snv | 3 | |||
rs28939086 | 0.925 | 0.160 | 7 | 107690220 | missense variant | A/C;G | snv | 2.0E-04; 4.0E-06 | 4 | ||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
rs104894378 | 0.882 | 0.120 | 12 | 114385521 | missense variant | C/G;T | snv | 6 | |||
rs104894381 | 0.925 | 0.120 | 12 | 114401830 | missense variant | C/T | snv | 5 | |||
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs121918502 | 0.790 | 0.160 | 10 | 121517351 | missense variant | G/C | snv | 9 | |||
rs77543610 | 0.667 | 0.560 | 10 | 121520160 | missense variant | G/C | snv | 28 | |||
rs104894232 | 0.925 | 0.160 | 11 | 125900000 | missense variant | A/G | snv | 1.1E-03 | 1.0E-03 | 4 | |
rs1057519321 | 0.807 | 0.160 | 5 | 128349391 | missense variant | C/A;T | snv | 7 | |||
rs4954218 | 0.925 | 0.080 | 2 | 135045855 | intron variant | G/T | snv | 0.83 | 5 | ||
rs4988235 | 0.752 | 0.400 | 2 | 135851076 | intron variant | G/A;C | snv | 19 | |||
rs1387329667 | 9 | 136500595 | missense variant | G/A | snv | 2 | |||||
rs756434709 | 9 | 136514670 | missense variant | C/T | snv | 2.0E-05 | 7.0E-06 | 2 | |||
rs137854438 | 1.000 | 0.080 | 8 | 143728570 | stop gained | A/T | snv | 2 | |||
rs587777570 | 1.000 | 2 | 148947018 | missense variant | G/A | snv | 4 | ||||
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs121912678 | 0.851 | 0.080 | 2 | 157774114 | missense variant | C/G;T | snv | 8 | |||
rs104893951 | 0.851 | 0.080 | 6 | 1610780 | missense variant | T/A;C | snv | 8.0E-06 | 5 | ||
rs142322800 | 1 | 161548502 | missense variant | T/C | snv | 1.5E-04 | 5.6E-05 | 1 | |||
rs1206736425 | 1 | 161626229 | missense variant | T/C | snv | 2 | |||||
rs1057517786 | 0.925 | 0.400 | 3 | 167704889 | stop gained | G/A | snv | 3 | |||
rs121913483 | 0.649 | 0.560 | 4 | 1801841 | missense variant | C/A;G;T | snv | 4.2E-06; 1.3E-05 | 31 |