Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1133763 | 0.882 | 0.200 | 17 | 34320812 | missense variant | A/C | snv | 0.21 | 0.15 | 4 | |
rs63750129 | 0.882 | 0.120 | 17 | 45996612 | missense variant | A/C | snv | 4.0E-06 | 4 | ||
rs1390191775 | 1.000 | 0.120 | X | 56564879 | missense variant | A/C;G | snv | 5.5E-06; 5.5E-06 | 1 | ||
rs1990622 | 0.742 | 0.200 | 7 | 12244161 | downstream gene variant | A/G | snv | 0.52 | 16 | ||
rs17125721 | 0.763 | 0.120 | 14 | 73206470 | missense variant | A/G | snv | 1.5E-02 | 1.5E-02 | 14 | |
rs4795541 | 0.807 | 0.200 | 17 | 30237299 | upstream gene variant | A/G | snv | 7 | |||
rs267607102 | 0.851 | 0.120 | 1 | 11022196 | missense variant | A/G | snv | 5 | |||
rs80356717 | 0.851 | 0.120 | 1 | 11018836 | missense variant | A/G | snv | 5 | |||
rs752076094 | 0.925 | 0.120 | 16 | 31185175 | missense variant | A/G | snv | 8.4E-06 | 2.8E-05 | 2 | |
rs63750092 | 0.882 | 0.120 | 17 | 46014277 | missense variant | A/T | snv | 3 | |||
rs3173615 | 0.807 | 0.200 | 7 | 12229791 | missense variant | C/A;G | snv | 0.49 | 12 | ||
rs63751180 | 0.882 | 0.120 | 17 | 44352087 | stop gained | C/A;G;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
rs741810 | 0.925 | 0.120 | 16 | 31182621 | synonymous variant | C/A;G;T | snv | 0.32; 4.0E-06; 4.0E-06 | 2 | ||
rs75932628 | 0.662 | 0.480 | 6 | 41161514 | missense variant | C/A;T | snv | 6.8E-05; 2.6E-03 | 28 | ||
rs750444386 | 0.807 | 0.360 | 12 | 117268082 | synonymous variant | C/A;T | snv | 4.0E-06; 5.6E-05 | 6 | ||
rs63751243 | 0.882 | 0.160 | 17 | 44349190 | missense variant | C/A;T | snv | 4.0E-06 | 4 | ||
rs17350674 | 1.000 | 0.120 | 9 | 34306412 | stop gained | C/A;T | snv | 0.16; 4.1E-06 | 1 | ||
rs1417841099 | 1.000 | 0.120 | 19 | 852917 | missense variant | C/G | snv | 4.6E-06 | 1 | ||
rs753009660 | 1.000 | 0.120 | X | 56564910 | missense variant | C/G | snv | 2.2E-05 | 3.8E-05 | 1 | |
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs63750349 | 0.851 | 0.200 | 17 | 45996638 | missense variant | C/G;T | snv | 4.0E-06 | 5 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs63751273 | 0.645 | 0.280 | 17 | 46010389 | missense variant | C/T | snv | 42 | |||
rs63750424 | 0.677 | 0.240 | 17 | 46024061 | missense variant | C/T | snv | 1.6E-05 | 30 |