Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs255012 | 1.000 | 0.200 | 7 | 41189487 | regulatory region variant | T/A;C | snv | 2 | |||
rs1364926780 | 0.882 | 0.200 | 7 | 87550272 | missense variant | C/T | snv | 5 | |||
rs199516560 | 0.851 | 0.200 | 7 | 87600772 | 5 prime UTR variant | G/A | snv | 2.1E-05 | 5 | ||
rs1404008939 | 0.925 | 0.200 | 7 | 87504324 | missense variant | A/C;G | snv | 4.0E-06 | 4 | ||
rs3740066 | 0.724 | 0.440 | 10 | 99844450 | missense variant | C/G;T | snv | 2.4E-05; 0.34 | 20 | ||
rs2273697 | 0.776 | 0.360 | 10 | 99804058 | missense variant | G/A | snv | 0.19 | 0.19 | 11 | |
rs730882213 | 0.925 | 0.080 | 19 | 1912477 | missense variant | G/A | snv | 7.0E-06 | 4 | ||
rs1445362103 | 1.000 | 0.040 | 13 | 111244248 | missense variant | T/C | snv | 1.2E-05 | 7.0E-06 | 2 | |
rs1378981995 | 0.925 | 0.200 | 3 | 94003751 | missense variant | G/A | snv | 7.0E-06 | 3 | ||
rs122460151 | 0.851 | 0.280 | X | 2958423 | missense variant | C/G | snv | 7.1E-05 | 3.8E-05 | 5 | |
rs104894743 | 0.807 | 0.200 | X | 25012937 | missense variant | G/A | snv | 7 | |||
rs121918822 | Y | 1642868 | missense variant | C/T | snv | 1 | |||||
rs387907281 | 0.752 | 0.280 | 19 | 41970284 | missense variant | C/T | snv | 13 | |||
rs587776690 | 0.882 | 0.280 | 3 | 142556439 | synonymous variant | T/C | snv | 4 | |||
rs1301785134 | 0.925 | 0.280 | 3 | 142556117 | missense variant | C/T | snv | 4.0E-06 | 3 | ||
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs180177035 | 0.752 | 0.280 | 7 | 140801502 | missense variant | T/C | snv | 35 | |||
rs4846049 | 0.776 | 0.360 | 1 | 11790308 | 3 prime UTR variant | T/A;G | snv | 11 | |||
rs118203933 | 0.925 | 0.360 | 8 | 85473779 | missense variant | C/T | snv | 8.0E-06 | 6 | ||
rs200115000 | 1.000 | 0.160 | 7 | 44220165 | missense variant | C/A;G;T | snv | 2.6E-04; 5.8E-05 | 2 | ||
rs397514627 | 0.882 | 0.160 | 10 | 73842486 | missense variant | C/A;G | snv | 5 | |||
rs10410239 | 1.000 | 0.200 | 19 | 13919876 | synonymous variant | T/C | snv | 0.27 | 0.38 | 2 | |
rs6511901 | 1.000 | 0.200 | 19 | 13916839 | intron variant | C/T | snv | 0.39 | 2 | ||
rs753303079 | 1 | 207325673 | missense variant | C/G;T | snv | 8.0E-06 | 1 |