Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs16944 | 0.531 | 0.920 | 2 | 112837290 | upstream gene variant | A/G | snv | 0.57 | 92 | ||
rs4994 | 0.578 | 0.640 | 8 | 37966280 | missense variant | A/G | snv | 0.11 | 9.2E-02 | 65 | |
rs9340799 | 0.583 | 0.680 | 6 | 151842246 | intron variant | A/G | snv | 0.32 | 62 | ||
rs2075650 | 0.662 | 0.360 | 19 | 44892362 | intron variant | A/G | snv | 0.13 | 0.13 | 45 | |
rs1799889 | 0.649 | 0.600 | 7 | 101126430 | upstream gene variant | A/G | snv | 31 | |||
rs1801260 | 0.695 | 0.280 | 4 | 55435202 | 3 prime UTR variant | A/G | snv | 0.25 | 28 | ||
rs334558 | 0.701 | 0.320 | 3 | 120094435 | upstream gene variant | A/G | snv | 0.51 | 20 | ||
rs10434 | 0.701 | 0.480 | 6 | 43785475 | 3 prime UTR variant | A/G | snv | 0.59 | 17 | ||
rs2230912 | 0.752 | 0.280 | 12 | 121184393 | missense variant | A/G | snv | 0.13 | 0.12 | 16 | |
rs9296158 | 0.763 | 0.080 | 6 | 35599305 | intron variant | A/G | snv | 0.65 | 16 | ||
rs4906902 | 0.724 | 0.200 | 15 | 26774621 | intron variant | A/G | snv | 0.15 | 14 | ||
rs2227631 | 0.742 | 0.200 | 7 | 101126257 | upstream gene variant | A/G | snv | 0.54 | 13 | ||
rs11030104 | 0.790 | 0.240 | 11 | 27662970 | intron variant | A/G | snv | 0.16 | 12 | ||
rs7997012 | 0.807 | 0.080 | 13 | 46837850 | intron variant | A/G | snv | 0.69 | 11 | ||
rs900418273 | 0.807 | 0.120 | 11 | 113393764 | missense variant | A/G | snv | 8 | |||
rs139315125 | 0.851 | 0.080 | 1 | 7809900 | missense variant | A/G | snv | 5.6E-03 | 5.0E-03 | 7 | |
rs1013940 | 0.827 | 0.160 | 2 | 107992192 | missense variant | A/G | snv | 9.3E-02 | 7.4E-02 | 6 | |
rs1409851868 | 0.882 | 0.080 | 3 | 89399325 | missense variant | A/G | snv | 6 | |||
rs2253206 | 0.851 | 0.080 | 2 | 207527254 | intron variant | A/G | snv | 0.47 | 6 | ||
rs3789327 | 0.925 | 0.080 | 11 | 13363769 | intron variant | A/G | snv | 0.53 | 6 | ||
rs13440581 | 0.882 | 0.080 | X | 151181399 | missense variant | A/G | snv | 0.45 | 0.45 | 5 | |
rs174697 | 0.851 | 0.080 | 22 | 19966309 | intron variant | A/G | snv | 0.88 | 5 | ||
rs561077 | 0.882 | 0.080 | X | 151181177 | missense variant | A/G | snv | 0.43 | 0.45 | 4 | |
rs1187329 | 0.925 | 0.080 | 9 | 84674365 | intron variant | A/G | snv | 0.52 | 3 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 |