Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1000113 | 0.925 | 0.040 | 5 | 150860514 | intron variant | C/T | snv | 0.13 | 1 | ||
rs1001007 | 0.827 | 0.120 | 3 | 46387167 | intron variant | A/G;T | snv | 5 | |||
rs10010325 | 1.000 | 0.040 | 4 | 105185196 | intron variant | C/A;G;T | snv | 3 | |||
rs1004234 | 0.827 | 0.120 | 5 | 132421409 | intron variant | A/G;T | snv | 5 | |||
rs1004819 | 0.776 | 0.360 | 1 | 67204530 | intron variant | G/A | snv | 0.30 | 1 | ||
rs10094579 | 0.807 | 0.280 | 8 | 89837077 | downstream gene variant | C/A | snv | 0.18 | 5 | ||
rs1016883 | 1.000 | 0.040 | 2 | 198016944 | intron variant | G/A | snv | 0.20 | 1 | ||
rs10174238 | 0.724 | 0.200 | 2 | 191108308 | intron variant | G/A | snv | 0.70 | 12 | ||
rs10185424 | 0.925 | 0.040 | 2 | 102046427 | intron variant | T/G | snv | 0.62 | 2 | ||
rs1047781 | 0.790 | 0.200 | 19 | 48703374 | missense variant | A/T | snv | 3.6E-02 | 1.2E-02 | 2 | |
rs1049526 | 0.925 | 0.040 | 6 | 32981027 | 3 prime UTR variant | C/T | snv | 0.93 | 3 | ||
rs1050152 | 0.776 | 0.480 | 5 | 132340627 | missense variant | C/T | snv | 0.29 | 0.28 | 1 | |
rs10510607 | 0.827 | 0.120 | 3 | 28244770 | intron variant | C/T | snv | 0.15 | 5 | ||
rs1052571 | 0.882 | 0.080 | 1 | 15524118 | missense variant | G/A | snv | 0.50 | 0.59 | 1 | |
rs10743181 | 0.827 | 0.120 | 11 | 2208529 | regulatory region variant | A/G | snv | 0.77 | 5 | ||
rs10748781 | 0.763 | 0.160 | 10 | 99523573 | upstream gene variant | C/A;G | snv | 11 | |||
rs10750899 | 0.827 | 0.120 | 11 | 58517478 | intergenic variant | G/A | snv | 0.95 | 5 | ||
rs10758669 | 0.763 | 0.280 | 9 | 4981602 | upstream gene variant | C/A;T | snv | 6 | |||
rs10761648 | 0.827 | 0.120 | 10 | 62594503 | intron variant | C/T | snv | 0.20 | 5 | ||
rs10761659 | 0.925 | 0.040 | 10 | 62685804 | intron variant | A/G | snv | 0.43 | 3 | ||
rs10775412 | 0.827 | 0.120 | 17 | 27542007 | intron variant | A/C | snv | 0.30 | 5 | ||
rs1077773 | 1.000 | 0.040 | 7 | 17403055 | intron variant | G/A;C | snv | 2 | |||
rs10781499 | 0.925 | 0.040 | 9 | 136371953 | synonymous variant | G/A | snv | 0.41 | 0.38 | 3 | |
rs10797432 | 1.000 | 0.040 | 1 | 2569899 | downstream gene variant | C/T | snv | 0.51 | 2 | ||
rs10800309 | 0.925 | 0.120 | 1 | 161502368 | upstream gene variant | A/G;T | snv | 2 |