Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 |
|
Digestive System Diseases | 0.900 | 0.944 | 36 | 2006 | 2020 | ||||||
|
0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 |
|
Digestive System Diseases | 0.900 | 0.773 | 22 | 2006 | 2020 | ||||||
|
0.776 | 0.360 | 1 | 67204530 | intron variant | G/A | snv | 0.30 |
|
Digestive System Diseases | 0.860 | 1.000 | 8 | 2006 | 2019 | |||||||
|
0.627 | 0.720 | 1 | 67259437 | 3 prime UTR variant | C/A | snv | 0.27 |
|
Digestive System Diseases | 0.850 | 1.000 | 7 | 2006 | 2020 | |||||||
|
0.716 | 0.440 | 1 | 67228519 | intron variant | A/G;T | snv |
|
Digestive System Diseases | 0.850 | 1.000 | 7 | 2006 | 2013 | ||||||||
|
0.752 | 0.320 | 1 | 67236843 | intron variant | T/G | snv | 4.4E-02 | 5.4E-02 |
|
Digestive System Diseases | 0.800 | 1.000 | 5 | 2006 | 2010 | ||||||
|
0.752 | 0.400 | 1 | 67253446 | intron variant | G/A | snv | 0.41 |
|
Digestive System Diseases | 0.800 | 1.000 | 3 | 2006 | 2007 | |||||||
|
0.689 | 0.600 | 1 | 67215986 | intron variant | T/G | snv | 0.37 |
|
Digestive System Diseases | 0.720 | 1.000 | 3 | 2006 | 2010 | |||||||
|
0.827 | 0.240 | 1 | 67222666 | intron variant | T/C | snv | 0.48 |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2006 | 2006 | |||||||
|
0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 |
|
Digestive System Diseases | 0.900 | 1.000 | 15 | 2007 | 2020 | ||||||
|
0.689 | 0.600 | 1 | 67215986 | intron variant | T/G | snv | 0.37 |
|
Digestive System Diseases | 0.880 | 1.000 | 11 | 2007 | 2019 | |||||||
|
0.776 | 0.360 | 1 | 67204530 | intron variant | G/A | snv | 0.30 |
|
Digestive System Diseases | 0.050 | 0.800 | 5 | 2007 | 2017 | |||||||
|
0.827 | 0.240 | 1 | 67209833 | intron variant | C/T | snv | 0.30 |
|
Digestive System Diseases | 0.810 | 1.000 | 3 | 2007 | 2012 | |||||||
|
0.776 | 0.360 | 1 | 67204530 | intron variant | G/A | snv | 0.30 |
|
Digestive System Diseases | 0.020 | 1.000 | 2 | 2007 | 2012 | |||||||
|
0.827 | 0.120 | 1 | 67256884 | intron variant | C/A;T | snv |
|
Digestive System Diseases | 0.800 | 1.000 | 2 | 2007 | 2016 | ||||||||
|
0.882 | 0.080 | 1 | 67157615 | intron variant | G/A;T | snv | 5.7E-02 |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 |
|
Digestive System Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
|
1.000 | 0.040 | 1 | 67219915 | intron variant | A/C;T | snv |
|
Digestive System Diseases | 0.800 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
1.000 | 0.040 | 1 | 67233571 | intron variant | T/A;C;G | snv |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
1.000 | 0.040 | 1 | 67187327 | intron variant | G/A | snv | 0.29 |
|
Digestive System Diseases | 0.800 | 1.000 | 1 | 2007 | 2007 | |||||||
|
1.000 | 0.040 | 1 | 67205233 | intron variant | G/A | snv | 0.37 |
|
Digestive System Diseases | 0.800 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.925 | 0.120 | 1 | 67219760 | intron variant | G/A | snv | 0.43 | 0.47 |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||||
|
1.000 | 0.040 | 1 | 67207082 | intron variant | G/A | snv | 0.33 | 0.30 |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||||
|
0.882 | 0.080 | 1 | 67260421 | downstream gene variant | T/C | snv | 0.13 |
|
Digestive System Diseases | 0.800 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 |
|
Musculoskeletal Diseases | 0.900 | 1.000 | 14 | 2008 | 2018 |