Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs673548 | 0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv | 10 | |||
rs1042034 | 0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 | 7 | |
rs2678379 | 1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 | 7 | ||
rs676210 | 0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 | 7 | ||
rs693 | 0.708 | 0.440 | 2 | 21009323 | synonymous variant | G/A | snv | 0.39 | 0.38 | 7 | |
rs533617 | 2 | 21011100 | missense variant | T/C | snv | 3.1E-02 | 2.9E-02 | 6 | |||
rs10199768 | 2 | 21021128 | intron variant | G/T | snv | 0.35 | 5 | ||||
rs1041968 | 2 | 21009932 | synonymous variant | G/A | snv | 0.39 | 0.38 | 4 | |||
rs1042031 | 0.790 | 0.200 | 2 | 21002881 | stop gained | C/A;T | snv | 8.0E-06; 0.15 | 3 | ||
rs12691202 | 2 | 21026844 | missense variant | C/T | snv | 2.7E-02 | 2.7E-02 | 3 | |||
rs12713956 | 2 | 21018633 | intron variant | A/G | snv | 0.14 | 3 | ||||
rs12720826 | 2 | 21042823 | intron variant | T/C | snv | 3.8E-02 | 3 | ||||
rs12720828 | 2 | 21018872 | intron variant | C/T | snv | 0.13 | 3 | ||||
rs12720838 | 2 | 21024339 | 3 prime UTR variant | C/T | snv | 0.14 | 3 | ||||
rs1367117 | 1.000 | 0.080 | 2 | 21041028 | missense variant | G/A | snv | 0.26 | 0.24 | 3 | |
rs1800479 | 2 | 21004511 | intron variant | C/G | snv | 0.16 | 0.17 | 3 | |||
rs1800481 | 2 | 21044338 | upstream gene variant | A/G | snv | 0.82 | 3 | ||||
rs2854725 | 2 | 21014914 | intron variant | T/A;G | snv | 3 | |||||
rs3749054 | 2 | 21014366 | intron variant | A/T | snv | 0.13 | 3 | ||||
rs520354 | 2 | 21036740 | intron variant | A/G | snv | 0.39 | 3 | ||||
rs531819 | 2 | 21040767 | intron variant | T/G | snv | 0.83 | 3 | ||||
rs550619 | 2 | 21037729 | intron variant | G/A | snv | 0.86 | 3 | ||||
rs570877 | 2 | 21028168 | intron variant | T/G | snv | 0.87 | 3 | ||||
rs5742904 | 0.689 | 0.280 | 2 | 21006288 | missense variant | C/A;T | snv | 2.8E-04 | 7.3E-04 | 3 | |
rs597331 | 2 | 21039555 | intron variant | G/A;T | snv | 3 |