Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11039149 | 0.827 | 0.280 | 11 | 47255124 | intron variant | A/G | snv | 0.19 | 4 | ||
rs9564966 | 0.851 | 0.120 | 13 | 73322084 | intergenic variant | A/G | snv | 0.52 | 4 | ||
rs1209809979 | 0.925 | 0.120 | 1 | 45568989 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
rs4619 | 0.882 | 0.160 | 7 | 45893070 | missense variant | A/G | snv | 0.36 | 0.38 | 3 | |
rs11085754 | 0.925 | 0.120 | 19 | 11017920 | intron variant | A/G | snv | 0.41 | 2 | ||
rs1318 | 0.925 | 0.120 | 17 | 67695266 | 3 prime UTR variant | A/G | snv | 0.30 | 2 | ||
rs138147246 | 0.925 | 0.120 | 3 | 9756551 | synonymous variant | A/G | snv | 8.0E-06 | 1.4E-05 | 2 | |
rs1810205 | 0.925 | 0.120 | 10 | 16923228 | intron variant | A/G | snv | 0.47 | 2 | ||
rs371609024 | 0.925 | 0.120 | 14 | 65629530 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
rs4149086 | 0.925 | 0.120 | 12 | 21239517 | 3 prime UTR variant | A/G | snv | 4.5E-04 | 2 | ||
rs4795218 | 0.925 | 0.120 | 17 | 37718512 | intron variant | A/G | snv | 0.82 | 2 | ||
rs747601652 | 0.925 | 0.120 | 1 | 74723233 | missense variant | A/G | snv | 1.2E-05 | 2 | ||
rs935821839 | 0.925 | 0.120 | 1 | 3727199 | missense variant | A/G | snv | 7.0E-06 | 2 | ||
rs4269383 | 0.882 | 0.120 | 6 | 155876368 | intergenic variant | A/G | snv | 0.37 | 1 | ||
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 114 | ||
rs11571836 | 0.827 | 0.200 | 13 | 32399302 | 3 prime UTR variant | A/G;T | snv | 6 | |||
rs7675998 | 0.827 | 0.360 | 4 | 163086668 | intergenic variant | A/G;T | snv | 4 | |||
rs1801272 | 0.807 | 0.240 | 19 | 40848628 | missense variant | A/T | snv | 2.0E-02 | 1.8E-02 | 6 | |
rs2980879 | 0.925 | 0.120 | 8 | 125469233 | intron variant | A/T | snv | 0.69 | 2 | ||
rs2736100 | 0.550 | 0.880 | 5 | 1286401 | 3 prime UTR variant | C/A | snv | 0.52 | 73 | ||
rs11554495 | 0.701 | 0.240 | 12 | 52904798 | missense variant | C/A | snv | 4.9E-03 | 5.4E-03 | 16 | |
rs74315364 | 0.732 | 0.200 | 1 | 182586014 | stop gained | C/A | snv | 3.6E-03; 4.0E-06 | 3.3E-03 | 13 | |
rs889312 | 0.732 | 0.360 | 5 | 56736057 | regulatory region variant | C/A | snv | 0.69 | 13 | ||
rs4988483 | 0.752 | 0.240 | 16 | 1079010 | missense variant | C/A | snv | 3.7E-02 | 3.7E-02 | 11 | |
rs9582036 | 0.776 | 0.280 | 13 | 28311271 | intron variant | C/A | snv | 0.59 | 8 |