Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 5 | |
rs2201841 | 0.716 | 0.440 | 1 | 67228519 | intron variant | A/G;T | snv | 4 | |||
rs11465759 | 1 | 67166721 | intron variant | T/G | snv | 2.4E-02 | 4 | ||||
rs11465804 | 0.752 | 0.320 | 1 | 67236843 | intron variant | T/G | snv | 4.4E-02 | 5.4E-02 | 3 | |
rs10889677 | 0.627 | 0.720 | 1 | 67259437 | 3 prime UTR variant | C/A | snv | 0.27 | 2 | ||
rs7517847 | 0.689 | 0.600 | 1 | 67215986 | intron variant | T/G | snv | 0.37 | 2 | ||
rs9988642 | 0.882 | 0.080 | 1 | 67260421 | downstream gene variant | T/C | snv | 0.13 | 2 | ||
rs10489629 | 0.827 | 0.240 | 1 | 67222666 | intron variant | T/C | snv | 0.48 | 1 | ||
rs7518660 | 0.925 | 0.120 | 1 | 67219760 | intron variant | G/A | snv | 0.43 | 0.47 | 1 | |
rs11804284 | 1.000 | 0.040 | 1 | 67233571 | intron variant | T/A;C;G | snv | 1 | |||
rs10889676 | 0.827 | 0.120 | 1 | 67256884 | intron variant | C/A;T | snv | 1 | |||
rs76418789 | 0.882 | 0.080 | 1 | 67182913 | missense variant | G/A | snv | 7.3E-03 | 4.5E-03 | 1 | |
rs11209008 | 0.882 | 0.080 | 1 | 67157615 | intron variant | G/A;T | snv | 5.7E-02 | 1 | ||
rs1343151 | 0.752 | 0.400 | 1 | 67253446 | intron variant | G/A | snv | 0.41 | 1 | ||
rs11465802 | 1.000 | 0.040 | 1 | 67219915 | intron variant | A/C;T | snv | 1 | |||
rs7539625 | 1.000 | 0.040 | 1 | 67207082 | intron variant | G/A | snv | 0.33 | 0.30 | 1 | |
rs1004819 | 0.776 | 0.360 | 1 | 67204530 | intron variant | G/A | snv | 0.30 | 1 | ||
rs2064689 | 1.000 | 0.040 | 1 | 67187327 | intron variant | G/A | snv | 0.29 | 1 | ||
rs2902440 | 1.000 | 0.040 | 1 | 67205233 | intron variant | G/A | snv | 0.37 | 1 | ||
rs11805303 | 0.827 | 0.240 | 1 | 67209833 | intron variant | C/T | snv | 0.30 | 1 |