Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1366026966 | 1.000 | 0.040 | 13 | 51939100 | missense variant | A/T | snv | 7.0E-06 | 1 | ||
rs200134167 | 1.000 | 0.040 | 15 | 45108105 | missense variant | C/T | snv | 2.5E-04 | 2.2E-04 | 1 | |
rs762143558 | 1.000 | 0.040 | X | 131277876 | missense variant | G/A | snv | 9.3E-05 | 9.5E-06 | 1 | |
rs755153760 | 1.000 | 0.040 | 9 | 131144504 | missense variant | G/A | snv | 1.6E-04 | 2.1E-05 | 1 | |
rs1252641479 | 1.000 | 0.040 | 13 | 111300800 | missense variant | T/G | snv | 4.0E-06 | 2 | ||
rs1286080173 | 0.925 | 0.160 | 13 | 51942551 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 2 | ||
rs376910645 | 0.925 | 0.160 | 13 | 51944162 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs749085322 | 0.925 | 0.160 | 13 | 51941132 | missense variant | T/C | snv | 4.0E-05 | 2.1E-05 | 2 | |
rs775541743 | 0.925 | 0.160 | 13 | 51942481 | missense variant | A/T | snv | 4.0E-06 | 2 | ||
rs769214 | 0.925 | 0.160 | 11 | 34438170 | upstream gene variant | G/A | snv | 0.61 | 2 | ||
rs761234173 | 1.000 | 0.040 | 16 | 83783345 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
rs70961709 | 1.000 | 0.040 | 3 | 186620652 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 3 | ||
rs111033690 | 0.882 | 0.120 | 9 | 34647858 | missense variant | C/G;T | snv | 4.0E-06; 2.5E-04 | 3 | ||
rs80359823 | 0.882 | 0.080 | 1 | 42929298 | missense variant | G/A | snv | 3 | |||
rs35457250 | 0.925 | 0.080 | 3 | 186620775 | missense variant | C/T | snv | 9.0E-03 | 8.1E-03 | 5 | |
rs80359825 | 0.790 | 0.360 | 1 | 42929009 | missense variant | G/A | snv | 7 | |||
rs80359826 | 0.807 | 0.120 | 1 | 42929018 | stop gained | G/A;T | snv | 4.0E-06 | 7 | ||
rs1566304640 | 0.827 | 0.280 | 13 | 77900593 | missense variant | G/A | snv | 8 | |||
rs4917 | 0.790 | 0.160 | 3 | 186619924 | missense variant | T/C | snv | 0.68 | 0.68 | 9 | |
rs149989682 | 0.790 | 0.240 | 16 | 2317763 | missense variant | T/A;C | snv | 2.3E-03 | 10 | ||
rs781214034 | 0.790 | 0.320 | 13 | 77903538 | missense variant | C/T | snv | 1.3E-04 | 2.8E-05 | 10 | |
rs121918474 | 0.763 | 0.320 | 3 | 93905799 | missense variant | T/C | snv | 2.8E-05 | 1.4E-05 | 11 | |
rs4918 | 0.763 | 0.400 | 3 | 186620593 | missense variant | G/A;C | snv | 0.67 | 12 | ||
rs587782995 | 0.708 | 0.360 | 5 | 140114480 | missense variant | T/C | snv | 42 | |||
rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 43 |