Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1039659576 | 0.689 | 0.520 | 1 | 236803473 | missense variant | A/G | snv | 21 | |||
rs104893951 | 0.851 | 0.080 | 6 | 1610780 | missense variant | T/A;C | snv | 8.0E-06 | 5 | ||
rs104894232 | 0.925 | 0.160 | 11 | 125900000 | missense variant | A/G | snv | 1.1E-03 | 1.0E-03 | 4 | |
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 | |||
rs1051740 | 0.592 | 0.760 | 1 | 225831932 | missense variant | T/C | snv | 0.32 | 0.27 | 56 | |
rs1052108705 | 6 | 31165217 | missense variant | C/T | snv | 4.1E-06 | 2.1E-05 | 3 | |||
rs1057517786 | 0.925 | 0.400 | 3 | 167704889 | stop gained | G/A | snv | 3 | |||
rs1057519320 | 0.807 | 0.160 | 15 | 48444574 | missense variant | G/A | snv | 7 | |||
rs1057519321 | 0.807 | 0.160 | 5 | 128349391 | missense variant | C/A;T | snv | 7 | |||
rs1206736425 | 1 | 161626229 | missense variant | T/C | snv | 2 | |||||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs121909173 | 0.851 | 0.240 | 3 | 57199901 | missense variant | C/G | snv | 2.8E-05 | 1.4E-05 | 5 | |
rs121909497 | 0.925 | 0.080 | 11 | 102955390 | missense variant | A/G | snv | 3 | |||
rs121912678 | 0.851 | 0.080 | 2 | 157774114 | missense variant | C/G;T | snv | 8 | |||
rs121912974 | 0.882 | 0.240 | 7 | 75983548 | missense variant | G/C | snv | 2.4E-04 | 2.2E-04 | 4 | |
rs121913483 | 0.649 | 0.560 | 4 | 1801841 | missense variant | C/A;G;T | snv | 4.2E-06; 1.3E-05 | 31 | ||
rs121913499 | 0.605 | 0.520 | 2 | 208248389 | missense variant | G/A;C;T | snv | 51 | |||
rs121918214 | 1.000 | 0.200 | 16 | 53873837 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs121918355 | 0.807 | 0.280 | 14 | 74555629 | stop gained | G/A;T | snv | 2.1E-05; 4.2E-06 | 7 | ||
rs121918502 | 0.790 | 0.160 | 10 | 121517351 | missense variant | G/C | snv | 9 | |||
rs12329305 | 2 | 19353152 | synonymous variant | C/A;T | snv | 1.6E-04; 5.5E-02 | 1 | ||||
rs1234344050 | 2 | 188984825 | missense variant | C/G | snv | 4.0E-06 | 2 | ||||
rs12720071 | 0.807 | 0.200 | 6 | 88141462 | 3 prime UTR variant | T/C | snv | 0.11 | 7 | ||
rs1359880314 | 0.763 | 0.320 | 21 | 45534541 | synonymous variant | C/T | snv | 1.6E-05 | 2.8E-05 | 12 |