Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 66 | |
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 47 | |
rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 47 | ||
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 43 | ||
rs5744680 | 0.851 | 0.120 | 5 | 75584065 | intron variant | G/A | snv | 0.55 | 18 | ||
rs116843064 | 0.776 | 0.160 | 19 | 8364439 | missense variant | G/A | snv | 1.3E-02 | 1.5E-02 | 16 | |
rs1042034 | 0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 | 15 | |
rs2954021 | 1.000 | 0.040 | 8 | 125469835 | intron variant | A/G | snv | 0.54 | 15 | ||
rs28601761 | 1.000 | 0.040 | 8 | 125487789 | intron variant | C/G | snv | 0.37 | 13 | ||
rs7679 | 0.925 | 0.160 | 20 | 45947863 | 3 prime UTR variant | T/C | snv | 0.13 | 9 | ||
rs115849089 | 8 | 20054859 | intergenic variant | G/A | snv | 9.8E-02 | 7 | ||||
rs12679834 | 8 | 19962922 | intron variant | T/C | snv | 9.4E-02 | 7 | ||||
rs863750 | 12 | 124020897 | intron variant | C/T | snv | 0.53 | 7 | ||||
rs112259268 | 17 | 43797377 | downstream gene variant | C/A | snv | 1.9E-02 | 6 | ||||
rs72959041 | 6 | 127133748 | intron variant | G/A | snv | 3.2E-02 | 5 | ||||
rs7140110 | 13 | 113841051 | non coding transcript exon variant | T/C | snv | 0.28 | 4 | ||||
rs4976033 | 5 | 68418419 | regulatory region variant | A/C;G;T | snv | 3 |