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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
12 | 124879441 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
12 | 124879441 | intron variant | C/A;T | snv |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
12 | 124841232 | intron variant | C/T | snv | 2.2E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
12 | 124869264 | intron variant | T/A | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
12 | 124869264 | intron variant | T/A | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
12 | 124822302 | intron variant | G/T | snv | 3.1E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
12 | 124822302 | intron variant | G/T | snv | 3.1E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
12 | 124831101 | intron variant | A/G | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
12 | 124831101 | intron variant | A/G | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.080 | 12 | 124853790 | intron variant | T/C | snv | 8.2E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 12 | 124853790 | intron variant | T/C | snv | 8.2E-02 |
|
Nervous System Diseases; Mental Disorders | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
12 | 124777047 | 3 prime UTR variant | C/T | snv | 0.55 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
12 | 124779741 | intron variant | T/A;G | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||||
|
12 | 124806310 | intron variant | A/T | snv | 0.58 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
12 | 124806310 | intron variant | A/T | snv | 0.58 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
12 | 124814309 | missense variant | T/C | snv | 1.1E-04 | 2.0E-04 |
|
0.700 | 0 | ||||||||||||
|
12 | 124807881 | missense variant | G/A | snv | 8.0E-06 | 6.3E-05 |
|
0.700 | 0 | ||||||||||||
|
12 | 124815064 | missense variant | G/A | snv |
|
0.700 | 0 | ||||||||||||||
|
0.882 | 0.080 | 12 | 124800125 | missense variant | G/A | snv | 9.9E-04 | 6.7E-04 |
|
0.700 | 0 | ||||||||||
|
0.763 | 0.160 | 12 | 124827879 | intron variant | G/C | snv | 0.32 |
|
Cardiovascular Diseases | 0.040 | 0.750 | 4 | 2010 | 2018 | |||||||
|
0.763 | 0.160 | 12 | 124827879 | intron variant | G/C | snv | 0.32 |
|
Cardiovascular Diseases | 0.040 | 0.750 | 4 | 2010 | 2018 | |||||||
|
0.763 | 0.160 | 12 | 124827879 | intron variant | G/C | snv | 0.32 |
|
Pathological Conditions, Signs and Symptoms | 0.030 | 1.000 | 3 | 2010 | 2018 | |||||||
|
0.752 | 0.200 | 12 | 124800202 | synonymous variant | A/G;T | snv | 0.59; 4.0E-06 |
|
Cardiovascular Diseases | 0.030 | 1.000 | 3 | 2013 | 2018 | |||||||
|
0.752 | 0.200 | 12 | 124800202 | synonymous variant | A/G;T | snv | 0.59; 4.0E-06 |
|
Cardiovascular Diseases | 0.030 | 0.333 | 3 | 2013 | 2018 | |||||||
|
0.763 | 0.160 | 12 | 124827879 | intron variant | G/C | snv | 0.32 |
|
Cardiovascular Diseases | 0.020 | 1.000 | 2 | 2017 | 2018 |