Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2740348 | 0.851 | 0.160 | 17 | 746695 | missense variant | G/C;T | snv | 0.85 | 6 | ||
rs121913516 | 1.000 | 0.080 | 4 | 54729353 | missense variant | C/T | snv | 4.0E-06 | 6 | ||
rs121908587 | 0.827 | 0.120 | 4 | 54278380 | missense variant | C/T | snv | 6 | |||
rs1360131632 | 0.827 | 0.080 | 17 | 42301316 | missense variant | C/T | snv | 4.0E-06 | 6 | ||
rs121913448 | 0.827 | 0.120 | 9 | 130862976 | missense variant | G/A | snv | 5 | |||
rs121913461 | 0.851 | 0.120 | 9 | 130862970 | missense variant | T/C | snv | 5 | |||
rs137852975 | 0.851 | 0.240 | 11 | 62692671 | stop gained | C/A | snv | 2.0E-05 | 1.4E-05 | 5 | |
rs267607040 | 0.851 | 0.320 | 18 | 44951948 | missense variant | G/A | snv | 5 | |||
rs267607042 | 0.851 | 0.320 | 18 | 44951942 | missense variant | G/A;C | snv | 5 | |||
rs6503691 | 0.827 | 0.200 | 17 | 42242072 | intron variant | C/T | snv | 0.26 | 5 | ||
rs4148356 | 0.851 | 0.120 | 16 | 16083418 | missense variant | G/A | snv | 2.3E-02 | 1.3E-02 | 4 | |
rs45511401 | 0.851 | 0.120 | 16 | 16079375 | missense variant | G/T | snv | 3.8E-02 | 3.6E-02 | 4 | |
rs1057519773 | 0.851 | 0.160 | 9 | 130872901 | missense variant | T/A;C;G | snv | 4 | |||
rs121913451 | 0.851 | 0.160 | 9 | 130872903 | missense variant | C/A;G | snv | 4 | |||
rs121913452 | 0.851 | 0.080 | 9 | 130873027 | missense variant | T/A;C;G | snv | 4 | |||
rs1060500091 | 0.882 | 0.120 | 3 | 128481887 | missense variant | A/C | snv | 4 | |||
rs267607038 | 0.882 | 0.320 | 18 | 44951952 | missense variant | T/C;G | snv | 8.0E-06 | 4 | ||
rs141157255 | 0.882 | 0.120 | 12 | 98659331 | missense variant | G/A | snv | 4.0E-05 | 2.8E-05 | 3 | |
rs3092856 | 0.882 | 0.120 | 11 | 108289005 | missense variant | C/T | snv | 1.2E-02 | 2.2E-02 | 3 | |
rs1407906280 | 0.882 | 0.120 | 12 | 68839467 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs1057519771 | 1.000 | 0.080 | 9 | 130872201 | missense variant | G/C | snv | 2 | |||
rs121913454 | 0.925 | 0.080 | 9 | 130874969 | missense variant | A/G | snv | 2 | |||
rs121913460 | 0.925 | 0.080 | 9 | 130862971 | missense variant | A/T | snv | 2 | |||
rs1314838108 | 0.925 | 0.160 | 9 | 130854977 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
rs111340708 | 0.925 | 0.080 | 12 | 111447548 | intron variant | TGGGGTGGGGTGGGG/-;TGGGG;TGGGGTGGGG;TGGGGTGGGGTGGGGTGGGG;TGGGGTGGGGTGGGGTGGGGTGGGG | delins | 0.52 | 2 |