Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4879809 | 0.882 | 0.120 | 9 | 34635601 | 3 prime UTR variant | T/A;C;G | snv | 1.1E-03; 1.00 | 3 | ||
rs695872 | 0.925 | 0.120 | 12 | 111599125 | synonymous variant | G/A | snv | 0.79 | 0.61 | 2 | |
rs695871 | 1.000 | 0.080 | 12 | 111599196 | missense variant | G/C | snv | 0.77 | 0.61 | 2 | |
rs2228576 | 0.851 | 0.160 | 12 | 6347896 | missense variant | T/A;C;G | snv | 4.5E-06; 0.69 | 4 | ||
rs3733242 | 1.000 | 0.080 | 4 | 76754352 | missense variant | C/A;T | snv | 2.4E-05; 0.46 | 1 | ||
rs11868035 | 0.763 | 0.200 | 17 | 17811787 | splice region variant | G/A | snv | 0.45 | 0.33 | 14 | |
rs2303565 | 1.000 | 0.080 | 2 | 218680586 | intron variant | T/C | snv | 0.43 | 0.56 | 1 | |
rs1130409 | 0.555 | 0.720 | 14 | 20456995 | missense variant | T/A;C;G | snv | 4.0E-06; 4.0E-06; 0.42 | 72 | ||
rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 157 | |
rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 113 | ||
rs850713 | 1.000 | 0.080 | 17 | 44350364 | intron variant | G/A;T | snv | 0.28; 4.0E-06 | 1 | ||
rs2279238 | 0.790 | 0.320 | 11 | 47260473 | missense variant | C/T | snv | 0.26 | 0.26 | 11 | |
rs10122902 | 1.000 | 0.080 | 9 | 27556782 | synonymous variant | G/A | snv | 0.24 | 0.21 | 1 | |
rs3732379 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 38 | |
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs2251644 | 1.000 | 0.080 | 14 | 102001510 | intron variant | A/G | snv | 0.17 | 0.21 | 1 | |
rs3732378 | 0.620 | 0.720 | 3 | 39265671 | missense variant | G/A | snv | 0.14 | 0.12 | 48 | |
rs11701 | 0.925 | 0.080 | 14 | 20693894 | synonymous variant | T/A;C;G | snv | 4.0E-06; 0.14 | 2 | ||
rs2529438 | 1.000 | 0.080 | 7 | 30595014 | synonymous variant | G/A;C | snv | 0.11 | 1 | ||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs742710 | 0.925 | 0.080 | 20 | 5923382 | missense variant | C/T | snv | 0.11 | 0.12 | 2 | |
rs11558538 | 0.695 | 0.400 | 2 | 138002079 | missense variant | C/T | snv | 1.0E-01 | 8.4E-02 | 19 | |
rs1800435 | 0.827 | 0.200 | 9 | 113391611 | missense variant | C/G | snv | 8.3E-02 | 6.1E-02 | 7 | |
rs8141797 | 0.882 | 0.120 | 22 | 24186073 | missense variant | A/G | snv | 8.1E-02 | 9.8E-02 | 3 | |
rs3806873 | 1.000 | 0.080 | 5 | 5462494 | missense variant | A/G | snv | 7.0E-02 | 3.4E-02 | 1 |